FDA 510(k)

INDONTINENCE PAD

K-Number: K853741 · 1985-11-14

Decision Date1985-11-14

Product Code

DecisionSubstantially Equivalent

Device Summary

INDONTINENCE PAD 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 1985-11-14 under 510(k) number K853741. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INDONTINENCE PAD?

INDONTINENCE PAD is a medical device that received FDA 510(k) clearance on 1985-11-14. The listed applicant is Beghin_Say Intl., Inc.. The 510(k) number is K853741.

When did INDONTINENCE PAD receive FDA 510(k) clearance?

INDONTINENCE PAD received FDA 510(k) clearance on 1985-11-14, under 510(k) number K853741.

Who is the listed applicant for INDONTINENCE PAD?

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

Related Clinical Trials

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Other records listing Beghin_Say Intl., Inc. as applicant

K853740KAY PLUS ADULT DIAPER K840482MALE INSERT SLIP

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.