Surgical Drape Clip #201

FDA 510(k) K790855 · C. Intl.

Substantially Equivalent

510(k) numberK790855

Submission

Device name
Surgical Drape Clip #201
Applicant
C. Intl.
Mchenry, IL, US
Received
May 4, 1979
Decision date
August 3, 1979
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
GDO – Applier, Surgical, Clip
Device class
Class I (low risk)
Regulation
21 CFR 878.4800
Specialty
General, Plastic Surgery

Other 510(k)s with product code GDO

510(k)DeviceApplicantDecision
K926199Uniclip Surgical Clip ApplierGDO · Traditional Unisurge, Inc.04/20/1993SE
K890941Modified Suture Disp. Endoscopic Surgical Clip AppGDO · Traditional United States Surgical, A Division of Tyco Healthc04/07/1989SE
K890159Towel ClipsGDO · Traditional Dhason Brothers, Inc.02/03/1989SE
K890233Suture Clip Applier/RemoverGDO · Traditional Kinetic Medical Products01/27/1989SE
K820837Disposable Multiple Ligating ClipGDO · Traditional ETHICON, Inc.05/28/1982SE
K812291Ethicon Multiple Ligating Clip ApplierGDO · Traditional ETHICON, Inc.09/11/1981SE
K792378Hemospenser Cartridge Cat. No. 523500-GDO · Traditional Edward Weck, Inc.12/06/1979SE
K791845Bayonet Heifetz Clip AppliersGDO · Traditional Edward Weck, Inc.10/17/1979SE
K791157360 Hemoclip AppliersGDO · Traditional Edward Weck, Inc.06/27/1979SE
K790990Reynolds Double Hemoclip AppliersGDO · Traditional Edward Weck, Inc.06/05/1979SE

More from Edward Weck, Inc.

510(k)DeviceDecision
K792494Catheterization ForcepGEN · Traditional 12/20/1979SE
K790853Easy-SpecKNA · Traditional 07/30/1979SE
K790852Vagi-SpecKNA · Traditional 07/30/1979SE
K790851Vagi-Press #401KOH · Traditional 07/30/1979SE
K790854Forceps #101 and #102GEN · Traditional 06/05/1979SE
K790856Proctoscope #501GCF · Traditional 05/29/1979SE

Questions and answers

When was Surgical Drape Clip #201 cleared by the FDA?

Surgical Drape Clip #201 (K790855) received a 510(k) decision of Substantially Equivalent on August 3, 1979, 91 days after the submission was received.

What is the product code of K790855?

The FDA product code is GDO – Applier, Surgical, Clip, a Class I (low risk) device regulated under 21 CFR 878.4800.