Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

CHICOPEE ADULT INCONTINENCE SHIELDS

K-Number: K880338 · 1988-03-31

ApplicantChicopee, Inc.
Decision Date1988-03-31
Product CodeEYQ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

CHICOPEE ADULT INCONTINENCE SHIELDS is the device name listed in this FDA 510(k) record. The listed applicant is Chicopee, Inc.. It received FDA 510(k) clearance on 1988-03-31 under 510(k) number K880338. 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 CHICOPEE ADULT INCONTINENCE SHIELDS?

CHICOPEE ADULT INCONTINENCE SHIELDS is a medical device that received FDA 510(k) clearance on 1988-03-31. The listed applicant is Chicopee, Inc.. The 510(k) number is K880338.

When did CHICOPEE ADULT INCONTINENCE SHIELDS receive FDA 510(k) clearance?

CHICOPEE ADULT INCONTINENCE SHIELDS received FDA 510(k) clearance on 1988-03-31, under 510(k) number K880338.

Who is the listed applicant for CHICOPEE ADULT INCONTINENCE SHIELDS?

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

What is the FDA product code for CHICOPEE ADULT INCONTINENCE SHIELDS?

The FDA product code for CHICOPEE ADULT INCONTINENCE SHIELDS 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

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.

↑