Medical Device Manufacturer · US , Miami , FL

Vitalcare Group, Inc. - FDA 510(k) Cleared Devices

8 submissions · 8 cleared · Since 1998

8

Total

8

Cleared

0

Denied

Vitalcare Group, Inc. has 8 FDA 510(k) cleared medical devices. Based in Miami, US.

Historical record: 8 cleared submissions from 1998 to 2006. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by Vitalcare Group, Inc. Filter by specialty or product code using the sidebar.

Vitalcare Group, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Vitalcare Group, Inc.

8 devices

1-8 of 8

Cleared May 05, 2006

OMI RETRACTABLE SAFETY SYRINGE

General Hospital · 112d

Cleared Aug 23, 2005

VITALCARE I.V. ADMINISTRATION SET

General Hospital · 134d

Cleared May 04, 2005

VITALCARE POWDER FREE SYNTHETIC VINYL EXAMINATION GLOVE

General Hospital · 391d

Cleared Aug 27, 2003

VITALCARE STERILEWATER AND 0.9% SODIUM CHLORIDE PRE-FILLED 10CC/30CC SYRINGES

Gastroenterology & Urology · 83d

Cleared Aug 04, 1999

VINYL POWDERED EXAM GLOVE / CAT.# 15-020

General Hospital · 28d

Cleared Feb 12, 1999

GAUZE, SPONGES, CAT # 11-003

General & Plastic Surgery · 168d

Cleared Dec 23, 1998

VITALCARE DISPOSABLE VAGINAL SPECULUM

Obstetrics & Gynecology · 63d

Cleared Dec 21, 1998

LATEX PATIENT EXAMINATION GLOVE, CAT. NO. 1000M POWDERED

General Hospital · 126d