510(K) CLEARANCES 51 ▲2RECALLS POSTED 25 ▲2CLASS I 1PMA DECISIONS 50 ▲13WEEK ENDING / FDA DATA AS OF
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K902157Unknown

Johnson & Johnson Dual Syringe Applicator

Johnson & Johnson MEDICAL GmbH, Arlington TX / Traditional, Unknown
FDA source (opens on fda.gov)

K902157 is the FDA 510(k) clearance record for JOHNSON & JOHNSON DUAL SYRINGE APPLICATOR, a class II device, cleared for Johnson & Johnson Medical, Inc. on under FDA product code FMF (Syringe, Piston). FDA records list 56 510(k) clearances for Johnson & Johnson Medical, Inc., from to . As of , FDA records show no recalls naming K902157.

Clearance record

Decision date
Received
(198 days to decision)
Product code
FMF Syringe, Piston
Regulation
21 CFR 880.5860
Device class
Class II
Review panel
General Hospital
Applicant
Johnson & Johnson Medical, Inc. P.O. Box 90130, Arlington TX
Third party review
No

Clearances, product code FMF

Trailing 12 months
13 clearances under product code FMF in the twelve months to November 2026, December 2025 the highest month at 4.
Show the numbers
Monthly 510(k) clearances under FDA product code FMF, trailing twelve months
MonthClearances
December 20254
January 20260
February 20261
March 20260
April 20261
May 20261
June 20262
July 20261
August 20263
September 20260
October 20260
November 20260