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)

KAY PLUS ADULT DIAPER

K-Number: K853740 · 1985-10-17

ApplicantBeghin_Say Intl., Inc.
Decision Date1985-10-17
Product CodeEYQ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

KAY PLUS ADULT DIAPER is the device name listed in this FDA 510(k) record. The listed applicant is Beghin_Say Intl., Inc.. It received FDA 510(k) clearance on 1985-10-17 under 510(k) number K853740. 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 KAY PLUS ADULT DIAPER?

KAY PLUS ADULT DIAPER is a medical device that received FDA 510(k) clearance on 1985-10-17. The listed applicant is Beghin_Say Intl., Inc.. The 510(k) number is K853740.

When did KAY PLUS ADULT DIAPER receive FDA 510(k) clearance?

KAY PLUS ADULT DIAPER received FDA 510(k) clearance on 1985-10-17, under 510(k) number K853740.

Who is the listed applicant for KAY PLUS ADULT DIAPER?

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

What is the FDA product code for KAY PLUS ADULT DIAPER?

The FDA product code for KAY PLUS 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 Beghin_Say Intl., 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.

K853741INDONTINENCE PADK840482MALE INSERT SLIP

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.

↑