510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K925039Substantially Equivalent

Safesnap Safety Syringe

U.S. Medical Instruments, Inc., San Diego CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K925039 is the FDA 510(k) clearance record for SAFESNAP SAFETY SYRINGE, a class II device, cleared for U.S. Medical Instruments, Inc. on under FDA product code MEG (Syringe, Antistick). FDA records list 2 510(k) clearances for U.S. Medical Instruments, Inc., from to . As of , FDA records show no recalls naming K925039.

Clearance record

Decision date
Received
(499 days to decision)
Product code
MEG Syringe, Antistick
Regulation
21 CFR 880.5860
Device class
Class II
Review panel
General Hospital
Applicant
U.S. Medical Instruments, Inc. 3500 Estudillo, San Diego CA
510(k) summary
Statement
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