FDA 510(k) FDA unclassified Substantially Equivalent 🇺🇸 United States

STERILIZATION PROCESS/VAGINAL SPONGE

K Number: K792628 · Decision Jan 11, 1980
Classifications
1
FEI Numbers
59
Registration Numbers
59
Same Product Code
270
Applicant Total
72
Review Days
23

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Basic Information

Device Name
STERILIZATION PROCESS/VAGINAL SPONGE
K Number
K792628
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Applicant
Procter & Gamble Mfg. Co.
Date Received
December 19, 1979
Decision Date
January 11, 1980
Product Code
EFQ
Advisory Committee
Unknown
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
EFQ Gauze/Sponge, Internal

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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. →