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FDA 510(k)

INCONTINENT PAD & BELT

K-Number: K810544 · 1981-03-11

ApplicantPrinciple Business Ent.
Decision Date1981-03-11
Product CodeEYQ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

INCONTINENT PAD & BELT is the device name listed in this FDA 510(k) record. The listed applicant is Principle Business Ent.. It received FDA 510(k) clearance on 1981-03-11 under 510(k) number K810544. 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 INCONTINENT PAD & BELT?

INCONTINENT PAD & BELT is a medical device that received FDA 510(k) clearance on 1981-03-11. The listed applicant is Principle Business Ent.. The 510(k) number is K810544.

When did INCONTINENT PAD & BELT receive FDA 510(k) clearance?

INCONTINENT PAD & BELT received FDA 510(k) clearance on 1981-03-11, under 510(k) number K810544.

Who is the listed applicant for INCONTINENT PAD & BELT?

The FDA 510(k) record lists Principle Business Ent. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INCONTINENT PAD & BELT?

The FDA product code for INCONTINENT PAD & BELT is EYQ.

Related Clinical Trials

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.

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Other records listing Principle Business Ent. as applicant

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.

K843869TRANQUILITYK810918ROLL-A-SET

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.K903342DEODORIZING AND SOUND MUFFLING ANAL PADBiological Resistance, Inc.K891686LIB SYSTEM, BABY/ADULT DIAPERIntera Corp.K885185INTERA SHIELD AND INTERA UNDERGARMENTIntera Corp.K883894DRIPRIDE PROVIDE SLIMWeyerhaeuser 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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