Data / Medical devices / France / Laboratoire CCD
Laboratoire CCD: FDA-registered device maker in PARIS Ile-de-France, France, 5 510(k) clearances
Laboratoire CCD is registered with the FDA (registration 3005136445) in PARIS Ile-de-France, France. It lists 5 device types. The FDA files 5 510(k) clearances under its listings, the newest dated June 8, 1999. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3005136445
- Address
- 36 rue Brunel, PARIS Ile-de-France, France, 75017
- Owner or operator
- LABORATOIRE CCD (10061040)
- Roles
- Specification developer
- First device listed
- August 2, 2019
- Registered through
- 2026
- Brand names listed
- CLASSIC ULTRASOFT 18 CM, CLASSIC ULTRASOFT 23 CM, CLASSIC ULTRASOFT MOCK 18 CM, CLASSIC ULTRASOFT MOCK 23 CM, ECHOGYN ® EMBRYOVIEW M 18 CM, ECHOGYN® EMBRYOVIEW M MOCK 18 CM, ECHOGYN® EMBRYOVIEW M MOCK 23 CM, ECHOGYN®EMBRYOVIEW M 23 CM and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Cap, Cervical | HDR | 2 | Specification developer | accessdata.fda.gov |
| Catheter, Assisted Reproduction | MQF | 2 | Specification developer | accessdata.fda.gov |
| Curette, Suction, Endometrial (And Accessories) | HHK | 2 | Specification developer | accessdata.fda.gov |
| Insufflator, Hysteroscopic | HIG | 2 | Specification developer | accessdata.fda.gov |
| Needle, Assisted Reproduction | MQE | 2 | Specification developer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| June 8, 1999 | K990913 | HOC SET WITH VALVE, HOC SET WITHOUT VALVE, HOC SET WITH VALVE - SOFT PLUG, HOC SET WITHOUT VALVE - SOFT PLUG, OPS WITHOU | MQE | Substantially Equivalent | Laboratoires Prodimed | accessdata.fda.gov |
| May 27, 1999 | K983604 | INTRA-UTERINE TRANSFER, INTRA-FOLOPIAN TRANSFER | MQF | Substantially Equivalent | Washington Regulatory Services | accessdata.fda.gov |
| March 5, 1990 | K894259 | REGISTER, A DISPOSABLE HYSTEROGRAPHY CUPULA | HIG | Substantially Equivalent | Washington Regulatory Services | accessdata.fda.gov |
| January 27, 1989 | K884696 | RESUBMITTED ARTIFICIAL INSEMINATION INSTRUMENT SET | HDR | Substantially Equivalent | Laboratoire Ccd C/O Washington Regulatory Services | accessdata.fda.gov |
| October 14, 1988 | K881456 | PIPELLE DE CORNIER ENDOMETRIAL SUCTION CURETTE | HHK | Substantially Equivalent | Laboratoire Ccd C/O Washington Regulatory Services | accessdata.fda.gov |
Compare with other makers
- All makers of Catheter, Assisted Reproduction
- All makers of Insufflator, Hysteroscopic
- All makers of Curette, Suction, Endometrial (And Accessories)
- All makers of Needle, Assisted Reproduction
- All makers of Cap, Cervical
Updated June 8, 1999. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.