Guaze Balls CAT.#601-720

FDA 510(k) K801999 · Pollak (Intl.), Ltd.

Substantially Equivalent

510(k) numberK801999

Submission

Device name
Guaze Balls CAT.#601-720
Applicant
Pollak (Intl.), Ltd.
Mchenry, IL, US
Received
August 20, 1980
Decision date
September 16, 1980
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
EFQ – Gauze/Sponge, Internal
Device class
Unclassified

Other 510(k)s with product code EFQ

510(k)DeviceApplicantDecision
K991757Non-Absorbable Gauze for External Use, Sterile and Non SterileEFQ · Traditional Furlong Industries08/12/1999SE
K991215Symtex Gauze Pads (1'S) and Symtex Gauze Sponges Sterile 2'S and Sterile 10'SEFQ · Traditional Symtex Healthcare Corp.06/11/1999SE
K990974Vitop DressingEFQ · Traditional Wonder & Bioenergy Hi-Tech America, Inc.06/09/1999SE
K990584Gauze Sponges: Laparotomy Sponge, X-Ray DetectableEFQ · Traditional Broadline Medical Industries04/23/1999SE
K984187Crosstex Non-Woven SpongesEFQ · Traditional Crosstex Intl.02/18/1999SE
K983016Gauze, Sponges, Cat # 11-003EFQ · Traditional Vitalcare Group, Inc.02/12/1999SE
K983348Dynarex Tracheostomy SpongeEFQ · Traditional Dynarex Corp.12/11/1998SE
K983450Starryshine Gauze SpongeEFQ · Traditional T.C. Dental Products, Inc.11/12/1998SE
K982648Joan IIEFQ · Traditional Celanese Acetate Co.09/30/1998SE
K980791Dumex Pak-Its Woven Ribbon PackingEFQ · Traditional Dumex Medical Surgical Products, Ltd.04/29/1998SE

More from Dumex Medical Surgical Products, Ltd.

510(k)DeviceDecision
K000227UmbicutHFW · Traditional 04/27/2000SE
K810049Pedicat*KMJ · Traditional 04/21/1981SE
K810050Vecafix*KGX · Traditional 03/26/1981SE
K802011Infussion Alarm System I.A.S. CAT.#1118FLN · Traditional 10/31/1980SE
K802009Flowclamp CAT.#1011 & 1012FKK · Traditional 10/31/1980SE
K802017Dressing Change Set CAT.#910-930KDD · Traditional 10/10/1980SE
K802007Pediwet=Guaze Impregnated with PetrolFRQ · Traditional 09/26/1980SE
K802022Sterile Guaze Swabs CAT.#301-420EFQ · Traditional 09/16/1980SE
K802021Pediband CAT.#195-197NAD · Traditional 09/16/1980SE
K802019Suture Removal Set CAT.#906KDD · Traditional 09/16/1980SE

Questions and answers

When was Guaze Balls CAT.#601-720 cleared by the FDA?

Guaze Balls CAT.#601-720 (K801999) received a 510(k) decision of Substantially Equivalent on September 16, 1980, 27 days after the submission was received.

What is the product code of K801999?

The FDA product code is EFQ – Gauze/Sponge, Internal, a Unclassified device.