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

TAMPON, RELY MODIFIED

K Number: K780243 · Decision Mar 2, 1978
Classifications
1
FEI Numbers
92
Registration Numbers
93
Same Product Code
188
Applicant Total
72
Review Days
17

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Basic Information

Device Name
TAMPON, RELY MODIFIED
K Number
K780243
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.5470
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Applicant
Procter & Gamble Mfg. Co.
Date Received
February 13, 1978
Decision Date
March 2, 1978
Product Code
HEB
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
HEB Tampon, Menstrual, Unscented

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (HEB), 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. →