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FDA 510(k)

DEODORIZING AND SOUND MUFFLING ANAL PAD

K-Number: K903342 · 1990-10-23

ApplicantBiological Resistance, Inc.
Decision Date1990-10-23
Product CodeEYQ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

DEODORIZING AND SOUND MUFFLING ANAL PAD is the device name listed in this FDA 510(k) record. The listed applicant is Biological Resistance, Inc.. It received FDA 510(k) clearance on 1990-10-23 under 510(k) number K903342. The device is classified under product code EYQ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DEODORIZING AND SOUND MUFFLING ANAL PAD?

DEODORIZING AND SOUND MUFFLING ANAL PAD is a medical device that received FDA 510(k) clearance on 1990-10-23. The listed applicant is Biological Resistance, Inc.. The 510(k) number is K903342.

When did DEODORIZING AND SOUND MUFFLING ANAL PAD receive FDA 510(k) clearance?

DEODORIZING AND SOUND MUFFLING ANAL PAD received FDA 510(k) clearance on 1990-10-23, under 510(k) number K903342.

Who is the listed applicant for DEODORIZING AND SOUND MUFFLING ANAL PAD?

The FDA 510(k) record lists Biological Resistance, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DEODORIZING AND SOUND MUFFLING ANAL PAD?

The FDA product code for DEODORIZING AND SOUND MUFFLING ANAL PAD is EYQ.

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Related Devices (Code: EYQ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K950784DRISTAR URINARY INCONTINENCE MANAGEMENT SYSTEMAdvanced Bioresearch Assoc.K932310KIT PAK INCONTINENT SKIN CARE KITKit Pak, Inc.K891686LIB SYSTEM, BABY/ADULT DIAPERIntera Corp.K885185INTERA SHIELD AND INTERA UNDERGARMENTIntera Corp.K883894DRIPRIDE PROVIDE SLIMWeyerhaeuser Co.K883895DRIPRIDE ULTRA INCONTINENT PADWeyerhaeuser Co.

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.

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