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FDA 510(k)

INCONTINENCE PAD OR ADULT DIAPER

K-Number: K820961 · 1982-04-16

ApplicantDafoe & Dafoe, Inc.
Decision Date1982-04-16
Product CodeEYQ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

INCONTINENCE PAD OR ADULT DIAPER is the device name listed in this FDA 510(k) record. The listed applicant is Dafoe & Dafoe, Inc.. It received FDA 510(k) clearance on 1982-04-16 under 510(k) number K820961. 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 INCONTINENCE PAD OR ADULT DIAPER?

INCONTINENCE PAD OR ADULT DIAPER is a medical device that received FDA 510(k) clearance on 1982-04-16. The listed applicant is Dafoe & Dafoe, Inc.. The 510(k) number is K820961.

When did INCONTINENCE PAD OR ADULT DIAPER receive FDA 510(k) clearance?

INCONTINENCE PAD OR ADULT DIAPER received FDA 510(k) clearance on 1982-04-16, under 510(k) number K820961.

Who is the listed applicant for INCONTINENCE PAD OR ADULT DIAPER?

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

What is the FDA product code for INCONTINENCE PAD OR ADULT DIAPER?

The FDA product code for INCONTINENCE PAD OR ADULT DIAPER 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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Dafoe & Dafoe, Inc. 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.

K820960MAXI & MINI SHIELDSK820962COTTON SWABSK800747BELTLESS MAXI, MINI & SUPER MAXI PADS

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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