Cover, Shoe Operating Room

FDA 510(k) K865023 · Ulti-Med Intl., Inc.

Substantially Equivalent

510(k) numberK865023

Submission

Device name
Cover, Shoe Operating Room
Applicant
Ulti-Med Intl., Inc.
Schaumburg, IL, US
Received
December 23, 1986
Decision date
January 12, 1987
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
FXP – Cover, Shoe, Operating-Room
Device class
Class I (low risk)
Regulation
21 CFR 878.4040
Specialty
General, Plastic Surgery

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K955835Fluid Barrier Boot Knee & Ankle-HighFXP · Traditional Instrument Makar, Inc.11/19/1996SE
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K932738Kappler Pro/Vent BootFXP · Traditional Kappler, Inc.03/29/1994SE
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K923176Surgical Instrument Kit, DisposableKDD · Traditional 06/17/1993SE
K923175Surgical Instrument Kit, DisposableFMC · Traditional 06/17/1993SE
K920989Surgical Instrument Kit, DisposableKDD · Traditional 10/19/1992SEKD
K922828Ulcer Wound TrayKKX · Traditional 09/28/1992SEKD
K914244Sterile Custom Surgical KitsKDD · Traditional 02/24/1992SEKD
K914431Absorbent FiberNAB · Traditional 12/04/1991SE
K912693Post Operative SpongeNAB · Traditional 10/04/1991SE
K912692Conforming BandageNAB · Traditional 10/04/1991SE
K904896Eye PadHMP · Traditional 12/05/1990SE

Questions and answers

When was Cover, Shoe Operating Room cleared by the FDA?

Cover, Shoe Operating Room (K865023) received a 510(k) decision of Substantially Equivalent on January 12, 1987, 20 days after the submission was received.

What is the product code of K865023?

The FDA product code is FXP – Cover, Shoe, Operating-Room, a Class I (low risk) device regulated under 21 CFR 878.4040.