FDA 510(k)

PATIENT UNDERPAD

K-Number: K813263 · 1981-11-27

Decision Date1981-11-27

Product CodeKME

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

PATIENT UNDERPAD is the device name listed in this FDA 510(k) record. The listed applicant is The Buckeye Cellulose Corp.. It received FDA 510(k) clearance on 1981-11-27 under 510(k) number K813263. The device is classified under product code KME. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PATIENT UNDERPAD?

PATIENT UNDERPAD is a medical device that received FDA 510(k) clearance on 1981-11-27. The listed applicant is The Buckeye Cellulose Corp.. The 510(k) number is K813263.

When did PATIENT UNDERPAD receive FDA 510(k) clearance?

PATIENT UNDERPAD received FDA 510(k) clearance on 1981-11-27, under 510(k) number K813263.

Who is the listed applicant for PATIENT UNDERPAD?

The FDA 510(k) record lists The Buckeye Cellulose Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PATIENT UNDERPAD?

The FDA product code for PATIENT UNDERPAD is KME.

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Other records listing The Buckeye Cellulose Corp. as applicant

K822925BOUNDARY SINGLE-USE GOWNS K823173ARRIRM SCRUB BRUSH/SPONGE K821564BOUNDARY PROCESS CHANGE K820758BOUNDARY SINGLE-USE CRANIOTOMY SHEET K820116BOUNDARY K813450BOUNDARY SINGLE-USE DRAPES

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Related Devices (Code: KME)

K042145READY-HEAT BLANKETTechtrade, LLC K944953OREX MEDICAL BEDDINGThantex Specialties, Inc.K933636DISPOSE-A-SHEETBelmac Healthcare Corp.K932539DOCTOR DOWN --RESCUE WRAPThree Dog Down K922143AMERICAN BURN SHEETAmerican Silk Sutures, Inc.K915303FOIL BABY BUNTINGGam Industries, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.