FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

ATTENDS INCONTINENT BRIEF

K Number: K873036 · Decision Jan 19, 1988
Classifications
1
FEI Numbers
417
Registration Numbers
418
Same Product Code
55
Applicant Total
72
Review Days
168

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Basic Information

Device Name
ATTENDS INCONTINENT BRIEF
K Number
K873036
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
876.5920
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Procter & Gamble Mfg. Co.
Date Received
August 4, 1987
Decision Date
January 19, 1988
Product Code
EYQ
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
EYQ Garment, Protective, For Incontinence

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (EYQ), ordered by most recent decision date.

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Other Clearances by Procter & Gamble Mfg. Co.

K Number Device Name
K873457 SCENTED OR SCENTED DEODORIZED MENSTRUAL PADS
K864673 UNSCENTED MENSTRUAL PAD
K861863 MODIFIED PROTECTIVE GARMENT
K862348 SINGLE-USE PATIENT UNDERPAD
K860598 MODIFIED PROTECTIVE GARMENT FOR INCONTINENTS
K853880 ATTENDS DISPOS. UNDERPAD
K853000 SCENTED ALWAYS PANTILINERS
K852985 UNSCENTED ALWAYS PANTILINERS
K850956 ALWAYS MAXIPADS - SCENTED
K850939 ALWAYS SUPER MAXIPAD-SCENTED
Search all 72 clearances from Procter & Gamble Mfg. Co. →