Bandage Compress

FDA 510(k) K912952 · Cal West Trading Co.

Substantially Equivalent

510(k) numberK912952

Submission

Device name
Bandage Compress
Applicant
Cal West Trading Co.
Santa Fe Springs, CA, US
Received
July 2, 1991
Decision date
October 4, 1991
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
NAB – Gauze / Sponge,Nonresorbable For External Use
Device class
Class I (low risk)
Regulation
21 CFR 878.4014
Specialty
General, Plastic Surgery

Other 510(k)s with product code NAB

510(k)DeviceApplicantDecision
K946015Ivalon External SpongeNAB · Traditional Ivalon02/27/1995SE
K940755Isolyer (4X4, 8PLY)NAB · Traditional Isolyer Co.05/02/1994SE
K931610Omnisorb II, Nonwoven Sponge, Sterile and NonNAB · Traditional Omni Mfg., Inc.06/24/1993SE
K925590Multi-Trauma DressingNAB · Traditional Gam Industries, Inc.04/08/1993SE
K926072K-Band and K-CrepeNAB · Traditional Parema , Ltd.03/19/1993SE
K915591Sterile Gauze PadsNAB · Traditional Eagle Medical, Inc.01/27/1993SE
K924650Gauze SpongesNAB · Traditional Dav-Mar Medical Products, Inc.01/11/1993SE
K923602Absorbent Pad -- ModificationNAB · Traditional Winfield Laboratories, Inc.12/07/1992SE
K923115ClinisorbNAB · Traditional Hermitage Hospital Products, Inc.11/23/1992SE
K923378Usp Type Vii Gauze SpongesNAB · Traditional E.W.A., Ltd.10/06/1992SE

More from E.W.A., Ltd.

510(k)DeviceDecision
K9503924-O2 Plus (CPR) Mouth Barrier, Catalog No. 08050CBP · Traditional 02/21/1995SE
K933756Magnashield CPR Mouth BarrierCBP · Traditional 01/05/1994SE
K920269Ez Gauze SpongeNAB · Traditional 04/22/1992SE
K914842Gauze Bandage RollNAB · Traditional 12/04/1991SE
K912950Compress DressingNAB · Traditional 10/04/1991SE
K912953Gauze CompressNAB · Traditional 09/30/1991SE
K912955Eye PadEFQ · Traditional 09/10/1991SE
K912954Stretch Gauze BandageNAB · Traditional 09/10/1991SE
K91295112-PLY Gauze PadNAB · Traditional 09/10/1991SE
K912949Triangular BANDAGE,40NAB · Traditional 09/06/1991SE

Questions and answers

When was Bandage Compress cleared by the FDA?

Bandage Compress (K912952) received a 510(k) decision of Substantially Equivalent on October 4, 1991, 94 days after the submission was received.

What is the product code of K912952?

The FDA product code is NAB – Gauze / Sponge,Nonresorbable For External Use, a Class I (low risk) device regulated under 21 CFR 878.4014.