Data / Medical devices / Panama / Grupo VH Corp.
Grupo VH Corp.: FDA-registered device maker in Ciudad de Panama, Panama, 2 510(k) clearances
Grupo VH Corp. is registered with the FDA (registration 3014389131) in Ciudad de Panama, Panama. It lists 2 device types. The FDA files 2 510(k) clearances under its listings, the newest dated October 21, 2010. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3014389131
- Address
- 43th Floor, Oceania Business Plaza Tower 2000, Street Punta Colon, Ciudad de Panama, Panama, 0816
- Owner or operator
- GRUPO VH CORP. (10057348)
- Roles
- Exporter to the US
- First device listed
- March 24, 2018
- Registered through
- 2026
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days | FOZ | 2 | Exporter to the US | accessdata.fda.gov |
| Oximeter | DQA | 2 | Exporter to the US | 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 |
|---|---|---|---|---|---|---|
| October 21, 2010 | K101896 | MASIMO LNCS/M-LNCS OXIMETRY SENSORS | DQA | Substantially Equivalent | Masimo Corporation | accessdata.fda.gov |
| August 20, 1999 | K990236 | MODIFICATION OF JELCO*,JELCO*-W AND JELCO* PLUS I.V. CATHETERS, CATHLON* I.V. CATHETERS, OPTIVA* I.V. CATHETERS, PROTECT | FOZ | Substantially Equivalent | Johnson & Johnson Medical, Div. of Ethicon, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
- All makers of Oximeter
Updated October 21, 2010. 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.