510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K060109Substantially Equivalent

Omi Retractable Safety Syringe

Vitalcare Group, Inc., Deer Field IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K060109 is the FDA 510(k) clearance record for OMI RETRACTABLE SAFETY SYRINGE, a class II device, cleared for Vitalcare Group, Inc. on under FDA product code MEG (Syringe, Antistick). FDA records list 8 510(k) clearances for Vitalcare Group, Inc., from to . As of , FDA records show no recalls naming K060109.

Clearance record

Decision date
Received
(112 days to decision)
Product code
MEG Syringe, Antistick
Regulation
21 CFR 880.5860
Device class
Class II
Review panel
General Hospital
Applicant
Vitalcare Group, Inc. P.O. Box 7007, Deer Field IL
510(k) summary
Summary PDF
Third party review
No

Clearances, product code MEG

Trailing 12 months
2 clearances under product code MEG in the twelve months to October 2026, December 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code MEG, trailing twelve months
MonthClearances
November 20250
December 20251
January 20260
February 20261
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260