Data / Medical devices / United States / Medical Packaging Corporation
Medical Packaging Corporation: FDA-registered device maker in Camarillo, CA, United States, 1 510(k) clearance
Medical Packaging Corporation is registered with the FDA (registration 2023790) in Camarillo, CA, United States. It lists 4 device types. The FDA files 1 510(k) clearance under its listings, the newest dated January 9, 1987. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 2023790
- Address
- 941 Avenida Acaso, Camarillo, CA, United States, 93012
- Owner or operator
- MEDICAL PACKAGING CORP. (2023790)
- Roles
- Contract manufacturer, Manufacturer
- First device listed
- November 17, 2004
- Registered through
- 2026
- Brand names listed
- Cytology Brush, General Biopsy Device, Swab Pouch, Torque Limiting Wrench
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Applicator, Absorbent Tipped, Sterile | KXG | 1 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
| Brush, Biopsy, General & Plastic Surgery | GEE | 1 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
| Spatula, Cervical, Cytological | HHT | 2 | Manufacturer | accessdata.fda.gov |
| Tools, Pacemaker Service | DTF | 1 | Contract manufacturer, Manufacturer | 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 |
|---|---|---|---|---|---|---|
| January 9, 1987 | K864323 | CYTOLOGY BRUSHES | HHT | Substantially Equivalent | Medical Packaging Corp. | accessdata.fda.gov |
Compare with other makers
- All makers of Applicator, Absorbent Tipped, Sterile
- All makers of Brush, Biopsy, General & Plastic Surgery
- All makers of Spatula, Cervical, Cytological
- All makers of Tools, Pacemaker Service
Updated January 9, 1987. 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.