FDA 510(k)

SINGLE-USE PATIENT UNDERPAD

K-Number: K862348 · 1986-07-02

Decision Date1986-07-02

Product CodeKME

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

SINGLE-USE PATIENT UNDERPAD is the device name listed in this FDA 510(k) record. The listed applicant is Procter & Gamble Mfg. Co.. It received FDA 510(k) clearance on 1986-07-02 under 510(k) number K862348. The device is classified under product code KME. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SINGLE-USE PATIENT UNDERPAD?

SINGLE-USE PATIENT UNDERPAD is a medical device that received FDA 510(k) clearance on 1986-07-02. The listed applicant is Procter & Gamble Mfg. Co.. The 510(k) number is K862348.

When did SINGLE-USE PATIENT UNDERPAD receive FDA 510(k) clearance?

SINGLE-USE PATIENT UNDERPAD received FDA 510(k) clearance on 1986-07-02, under 510(k) number K862348.

Who is the listed applicant for SINGLE-USE PATIENT UNDERPAD?

The FDA 510(k) record lists Procter & Gamble Mfg. Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SINGLE-USE PATIENT UNDERPAD?

The FDA product code for SINGLE-USE PATIENT UNDERPAD is KME.

Related Clinical Trials

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Other records listing Procter & Gamble Mfg. Co. as applicant

K873457SCENTED OR SCENTED DEODORIZED MENSTRUAL PADS K873036ATTENDS INCONTINENT BRIEF K864673UNSCENTED MENSTRUAL PAD K861863MODIFIED PROTECTIVE GARMENT K860598MODIFIED PROTECTIVE GARMENT FOR INCONTINENTS K853880ATTENDS DISPOS. UNDERPAD

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Related Devices (Code: KME)

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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.