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FDA 510(k)

UNDERPAD, DISPOSABLE POLYPROPY. (UNILUX)

K-Number: K760164 · 1976-07-20

ApplicantParke-Davis Co.
Decision Date1976-07-20
Product CodeEYQ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

UNDERPAD, DISPOSABLE POLYPROPY. (UNILUX) is the device name listed in this FDA 510(k) record. The listed applicant is Parke-Davis Co.. It received FDA 510(k) clearance on 1976-07-20 under 510(k) number K760164. 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 UNDERPAD, DISPOSABLE POLYPROPY. (UNILUX)?

UNDERPAD, DISPOSABLE POLYPROPY. (UNILUX) is a medical device that received FDA 510(k) clearance on 1976-07-20. The listed applicant is Parke-Davis Co.. The 510(k) number is K760164.

When did UNDERPAD, DISPOSABLE POLYPROPY. (UNILUX) receive FDA 510(k) clearance?

UNDERPAD, DISPOSABLE POLYPROPY. (UNILUX) received FDA 510(k) clearance on 1976-07-20, under 510(k) number K760164.

Who is the listed applicant for UNDERPAD, DISPOSABLE POLYPROPY. (UNILUX)?

The FDA 510(k) record lists Parke-Davis Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for UNDERPAD, DISPOSABLE POLYPROPY. (UNILUX)?

The FDA product code for UNDERPAD, DISPOSABLE POLYPROPY. (UNILUX) is EYQ.

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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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