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

ADULT INCONTINENCE BRIEF

K Number: K834296 · Decision Feb 4, 1984
Classifications
1
FEI Numbers
417
Registration Numbers
418
Same Product Code
55
Applicant Total
72
Review Days
58

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
ADULT INCONTINENCE BRIEF
K Number
K834296
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
December 8, 1983
Decision Date
February 4, 1984
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.

View all

Other Clearances by Procter & Gamble Mfg. Co.

K Number Device Name
K873457 SCENTED OR SCENTED DEODORIZED MENSTRUAL PADS
K873036 ATTENDS INCONTINENT BRIEF
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
Search all 72 clearances from Procter & Gamble Mfg. Co. →