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FDA 510(k)

ULTRA SHIELD BRIEFS

K-Number: K841953 · 1984-07-19

ApplicantIpco Corp.
Decision Date1984-07-19
Product CodeEYQ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ULTRA SHIELD BRIEFS is the device name listed in this FDA 510(k) record. The listed applicant is Ipco Corp.. It received FDA 510(k) clearance on 1984-07-19 under 510(k) number K841953. 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 ULTRA SHIELD BRIEFS?

ULTRA SHIELD BRIEFS is a medical device that received FDA 510(k) clearance on 1984-07-19. The listed applicant is Ipco Corp.. The 510(k) number is K841953.

When did ULTRA SHIELD BRIEFS receive FDA 510(k) clearance?

ULTRA SHIELD BRIEFS received FDA 510(k) clearance on 1984-07-19, under 510(k) number K841953.

Who is the listed applicant for ULTRA SHIELD BRIEFS?

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

What is the FDA product code for ULTRA SHIELD BRIEFS?

The FDA product code for ULTRA SHIELD BRIEFS is EYQ.

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Other records listing Ipco Corp. as applicant

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Related Devices (Code: EYQ)

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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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