MULTIPLE STERILE GAUZE BANDAGE ROLLS, VARI SIZES— 510(k) K915821

Name: FDA 510(k) clearance K915821
Creator: U.S. Food and Drug Administration
Published: 1992-05-29

Substantially Equivalent

Kerma Medical Products, Inc.

FDA 510(k) clearance K915821 for MULTIPLE STERILE GAUZE BANDAGE ROLLS, VARI SIZES, Substantially Equivalent on 1992-05-29. Applicant: Kerma Medical Products, Inc.. Device class: 1.

Clearance details

Applicant: Kerma Medical Products, Inc.
Product code: Code NAB
Device class: Class 1
Regulation: 21 CFR 878.4014
Advisory panel: General, Plastic Surgery
Date received: 1991-12-30
Decision date: 1992-05-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Chesapeake, VA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code NAB

view all

K946015 — IVALON EXTERNAL SPONGE1995-02-27
K940755 — ISOLYER (4X4, 8PLY)1994-05-02
K931610 — OMNISORB II, NONWOVEN SPONGE, STERILE AND NON1993-06-24
K925590 — MULTI-TRAUMA DRESSING1993-04-08
K926072 — K-BAND AND K-CREPE1993-03-19

More clearances from Kerma Medical Products, Inc.

view all

K931042 — MOORE SECURE CAP1994-04-13
K915822 — MULTIPLE DRESSING, STERILE NONADDHERENT PADS1992-03-26
K914071 — MULTIPLE BURN DRESSING1991-12-04
K914937 — STERILE BANDAGE, GAUZE, FINE MESH, 3X8 INCHES1991-12-04

Data sourced from openFDA. This site is unofficial and independent of the FDA.