Bindafix

FDA 510(k) K791211 · Conphar, Inc.

Substantially Equivalent

510(k) numberK791211

Submission

Device name
Bindafix
Applicant
Conphar, Inc.
Mchenry, IL, US
Received
July 2, 1979
Decision date
August 3, 1979
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
FQM – Bandage, Elastic
Device class
Class I (low risk)
Regulation
21 CFR 880.5075
Specialty
General Hospital

Other 510(k)s with product code FQM

510(k)DeviceApplicantDecision
K040936Petit Silma Elastic Bandage with Germanium/Titanium OxideFQM · Traditional Leda Co., Ltd.05/03/2004SE
K040054Back in Action Compression & Support with Magnets for the Lower Back, Knee and AnkleFQM · Traditional Theodore Barash04/27/2004SE
K013244Comfortcare Compression Support Witih Magnets and Aegis Microbe Shield Comfortcare…FQM · Traditional Med Gen, Inc.12/07/2001SE
K952738Skin Saver SystemsFQM · Traditional Skin Saver Systems, Inc.09/29/1995SE
K872868Aspen Esmark BandageFQM · Traditional Aspen Laboratories, Inc.07/31/1987SE
K840107Tube-Bandage for Human Digits 200FQM · Traditional Zens Health Care Products04/25/1984SE
K831728MedicalexFQM · Traditional Medicalex01/09/1984SE
K830622Ortho WrapFQM · Traditional Fast Wrap Co., Inc.06/20/1983SE
K831551Compressogrip Tubular Elastic BandageFQM · Traditional Fred Sammons, Inc.06/07/1983SE
K820142Tubular StockinetteFQM · Traditional Stan-Pak Ent.02/05/1982SE

More from Stan-Pak Ent.

510(k)DeviceDecision
K821825Conphar Silicone Feeding TubeKNT · Traditional 08/10/1982SE
K821354Conphar Mayo Hegar Needle HolderGDF · Traditional 06/03/1982SE
K821295Olsen Hegar Needle HoldersGDF · Traditional 06/03/1982SE
K821289Mayo-Hegar Needle HolderGDF · Traditional 06/03/1982SE
K821298Backhaus Clamp, 3 1/2HTD · Traditional 05/28/1982SE
K821294Tonsil Scissors Straight 5 1/2EGN · Traditional 05/28/1982SE
K821293Backhaus Clamp, 5 1/4HTD · Traditional 05/28/1982SE
K821292Tonsil Scissors 7EGN · Traditional 05/28/1982SE
K821290Littauer Scissors 5 1/2HNF · Traditional 05/28/1982SE
K821286Iris Scissors Straight 4 1/2HNF · Traditional 05/28/1982SE

Questions and answers

When was Bindafix cleared by the FDA?

Bindafix (K791211) received a 510(k) decision of Substantially Equivalent on August 3, 1979, 32 days after the submission was received.

What is the product code of K791211?

The FDA product code is FQM – Bandage, Elastic, a Class I (low risk) device regulated under 21 CFR 880.5075.