FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

SCENTED ALWAYS PANTILINERS

K Number: K853000 · Decision Sep 6, 1985
Classifications
1
FEI Numbers
22
Registration Numbers
22
Same Product Code
56
Applicant Total
72
Review Days
53

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Basic Information

Device Name
SCENTED ALWAYS PANTILINERS
K Number
K853000
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.5425
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Applicant
Procter & Gamble Mfg. Co.
Date Received
July 15, 1985
Decision Date
September 6, 1985
Product Code
HHL
Advisory Committee
Obstetrics/Gynecology
Review Advisory Committee
OB
Third Party
N

Classifications

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

Product Code Device Name
HHL Pad, Menstrual, Scented, Scented-Deodorized

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (HHL), 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
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
K852985 UNSCENTED ALWAYS PANTILINERS
K850956 ALWAYS MAXIPADS - SCENTED
K850939 ALWAYS SUPER MAXIPAD-SCENTED
Search all 72 clearances from Procter & Gamble Mfg. Co. →