GAHClass I

Stylet, Surgical, General & Plastic Surgery

21 CFR 878.4800 / General, Plastic Surgery

GAH is the FDA product code for Stylet, Surgical, General & Plastic Surgery, a class I device type, regulated under 21 CFR 878.4800. As of 2026-09-10, FDA records hold 7 510(k) clearances under this code, the most recent dated 2011-04-22, and 3 recalls.

Classification record

Product code: GAH
Device name: Stylet, Surgical, General & Plastic Surgery
Regulation: 21 CFR 878.4800
Device class: Class I
Review panel: General, Plastic Surgery
Submission type: 510(k) exempt
Implant: No
Life sustaining or supporting: No
GMP exempt: No
Third party review eligible: No
Ingested clearances: 7
Ingested recalls: 3

Clearances, product code GAH

By decision year

7 clearances under product code GAH with a decision year between 1977 and 2011, 1997 the highest year at 3.

Show the numbers

510(k) clearances under FDA product code GAH by decision year
Year	Clearances
1977	1
1995	1
1997	3
2000	1
2011	1

Applicants with the most clearances

Product code GAH

Applicants holding the most 510(k) clearances under product code GAH
Applicant	Clearances
Advanced Medical Products, Inc.	1
Apex Medical Products, LLC	1
Barry Markman, M.D.	1
Medicamat S.A.	1
Padgett Instruments, Inc.	1
Sil-Med Corp.	1
Venx, LLC	1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 90 companies shown, in name order