Stockinette, Sterile Two Ply W/Pull Tabs

FDA 510(k) K801532 · The Owenby Co.

Substantially Equivalent

510(k) numberK801532

Submission

Device name
Stockinette, Sterile Two Ply W/Pull Tabs
Applicant
The Owenby Co.
Mchenry, IL, US
Received
July 1, 1980
Decision date
July 28, 1980
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

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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
K801628Restraint, ProtectiveIQK · Traditional 08/07/1980SE
K801627Cover, LimbIPM · Traditional 07/28/1980SE
K801626Arm SlingILI · Traditional 07/28/1980SE
K801531Arm SlingILI · Traditional 07/21/1980SE
K790210Stockinette, Tubular UnbleachedFQM · Traditional 02/27/1979SE
K780764Non-Sterile Folded GauzeNAB · Traditional 06/06/1978SE
K780418Burn Dressing PadFPY · Traditional 04/10/1978SE
K770889Burn Dressing KitEFQ · Traditional 07/11/1977SE
K761071P.S.M. Justa KapFYF · Traditional 12/30/1976SE
K761070P.S.M. Surgical HoodFXY · Traditional 12/30/1976SE

Questions and answers

When was Stockinette, Sterile Two Ply W/Pull Tabs cleared by the FDA?

Stockinette, Sterile Two Ply W/Pull Tabs (K801532) received a 510(k) decision of Substantially Equivalent on July 28, 1980, 27 days after the submission was received.

What is the product code of K801532?

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