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FDA 510(k)

MODIFIED PROTECTIVE GARMENT

K-Number: K861863 · 1986-08-11

ApplicantProcter & Gamble Mfg. Co.
Decision Date1986-08-11
Product CodeEYQ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MODIFIED PROTECTIVE GARMENT 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 1986-08-11 under 510(k) number K861863. 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 MODIFIED PROTECTIVE GARMENT?

MODIFIED PROTECTIVE GARMENT is a medical device that received FDA 510(k) clearance on 1986-08-11. The listed applicant is Procter & Gamble Mfg. Co.. The 510(k) number is K861863.

When did MODIFIED PROTECTIVE GARMENT receive FDA 510(k) clearance?

MODIFIED PROTECTIVE GARMENT received FDA 510(k) clearance on 1986-08-11, under 510(k) number K861863.

Who is the listed applicant for MODIFIED PROTECTIVE GARMENT?

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 MODIFIED PROTECTIVE GARMENT?

The FDA product code for MODIFIED PROTECTIVE GARMENT is EYQ.

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Other records listing Procter & Gamble Mfg. Co. 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.

K873457SCENTED OR SCENTED DEODORIZED MENSTRUAL PADSK873036ATTENDS INCONTINENT BRIEFK864673UNSCENTED MENSTRUAL PADK862348SINGLE-USE PATIENT UNDERPADK860598MODIFIED PROTECTIVE GARMENT FOR INCONTINENTSK853880ATTENDS DISPOS. UNDERPAD

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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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