Vitalcare Group, Inc.
Miami, FL, US
Vitalcare Group, Inc. appears in FDA device records in Miami, FL. FDA records list 8 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 8
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 8 510(k) clearances for Vitalcare Group, Inc. between 1998 and 2006. The busiest year on record is 1998, with 2. The most recent is 2006, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1998 | 2 |
| 1999 | 2 |
| 2003 | 1 |
| 2005 | 2 |
| 2006 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K060109 | OMI RETRACTABLE SAFETY SYRINGE | MEG | Substantially Equivalent | |
| K050906 | VITALCARE I.V. ADMINISTRATION SET | FPA | Substantially Equivalent | |
| K040916 | VITALCARE POWDER FREE SYNTHETIC VINYL EXAMINATION GLOVE | LYZ | Substantially Equivalent | |
| K031748 | VITALCARE STERILEWATER AND 0.9% SODIUM CHLORIDE PRE-FILLED 10CC/30CC SYRINGES | EZL | Substantially Equivalent | |
| K992289 | VINYL POWDERED EXAM GLOVE / CAT.# 15-020 | LYZ | Substantially Equivalent | |
| K983016 | GAUZE, SPONGES, CAT # 11-003 | EFQ | Substantially Equivalent | |
| K983716 | VITALCARE DISPOSABLE VAGINAL SPECULUM | HIB | Substantially Equivalent | |
| K982901 | LATEX PATIENT EXAMINATION GLOVE, CAT. NO. 1000M POWDERED | LYY | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain