Elastic Bandage

FDA 510(k) K843056 · Sterile Medical Systems

Substantially Equivalent

510(k) numberK843056

Submission

Device name
Elastic Bandage
Applicant
Sterile Medical Systems
South Weymouth, MA, US
Received
August 3, 1984
Decision date
December 4, 1984
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
GAX – Tourniquet, Nonpneumatic
Device class
Class I (low risk)
Regulation
21 CFR 878.5900
Specialty
General, Plastic Surgery

Other 510(k)s with product code GAX

510(k)DeviceApplicantDecision
K931198UniquetGAX · Traditional Icat Systems09/01/1993SE
K881398TourniquetGAX · Traditional Barretta Products, Research and Development, Inc.04/29/1988SE
K881176Sterile Esmarch BandageGAX · Traditional Spectrum/Hydro-Med Products, Inc.04/11/1988SE
K875092Degania Silicone TourniquetGAX · Traditional Degania Silicone , Ltd.01/07/1988SE
K873928Universal TourniquetGAX · Traditional Dryden Corp.10/23/1987SE
K872003KinderwrapGAX · Traditional The Kinder Co.06/23/1987SE
K864897Dale Venipuncture Tourniquet, Product No. 1335GAX · Traditional Dale Medical Products, Inc.01/12/1987SE
K853472Finger TourniquetteGAX · Traditional Joseph B. Marogil10/10/1985SE
K853537Velcro TourniquetGAX · Traditional Cp Medical09/12/1985SE
K852277Catapress TourniguetGAX · Traditional Boehringer Ingelheim Pharmaceuticals, Inc.06/27/1985SE

Questions and answers

When was Elastic Bandage cleared by the FDA?

Elastic Bandage (K843056) received a 510(k) decision of Substantially Equivalent on December 4, 1984, 123 days after the submission was received.

What is the product code of K843056?

The FDA product code is GAX – Tourniquet, Nonpneumatic, a Class I (low risk) device regulated under 21 CFR 878.5900.