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

PANTY-LINERS UNSCENTED

K Number: K830145 · Decision Jan 21, 1983
Classifications
1
FEI Numbers
307
Registration Numbers
307
Same Product Code
135
Applicant Total
72
Review Days
4

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Basic Information

Device Name
PANTY-LINERS UNSCENTED
K Number
K830145
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
884.5435
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Applicant
Procter & Gamble Mfg. Co.
Date Received
January 17, 1983
Decision Date
January 21, 1983
Product Code
HHD
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
HHD Pad, Menstrual, Unscented

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (HHD), 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
K853000 SCENTED ALWAYS PANTILINERS
K852985 UNSCENTED ALWAYS PANTILINERS
K850956 ALWAYS MAXIPADS - SCENTED
Search all 72 clearances from Procter & Gamble Mfg. Co. →