FDA 510(k)

MALE URINARY STRESS PAD*

K-Number: K862877 · 1986-11-19

ApplicantConvatec, A Division of E.R. Squibb & Sons

Decision Date1986-11-19

Product CodeEYQ

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

MALE URINARY STRESS PAD* is the device name listed in this FDA 510(k) record. The listed applicant is Convatec, A Division of E.R. Squibb & Sons. It received FDA 510(k) clearance on 1986-11-19 under 510(k) number K862877. 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 MALE URINARY STRESS PAD*?

MALE URINARY STRESS PAD* is a medical device that received FDA 510(k) clearance on 1986-11-19. The listed applicant is Convatec, A Division of E.R. Squibb & Sons. The 510(k) number is K862877.

When did MALE URINARY STRESS PAD* receive FDA 510(k) clearance?

MALE URINARY STRESS PAD* received FDA 510(k) clearance on 1986-11-19, under 510(k) number K862877.

Who is the listed applicant for MALE URINARY STRESS PAD*?

The FDA 510(k) record lists Convatec, A Division of E.R. Squibb & Sons as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MALE URINARY STRESS PAD*?

The FDA product code for MALE URINARY STRESS PAD* is EYQ.

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Other records listing Convatec, A Division of E.R. Squibb & Sons as applicant

K013814ABSORBENT ANTIMICROBIAL WOUND DRESSING K990964SIGNADRESS DUODERM DRESSING K984388HA ABSORBENT WOUND DRESSING K980720NONWOVEN PAD K980382NON-WOVEN COMPRESS K974823NONWOVEN DRESSING

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Related Devices (Code: EYQ)

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.