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

STERI-CLENS

K Number: K875129 · Decision Feb 18, 1988
Classifications
1
FEI Numbers
126
Registration Numbers
126
Same Product Code
36
Applicant Total
10
Review Days
65

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Basic Information

Device Name
STERI-CLENS
K Number
K875129
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Absorbent Cotton Co., Inc.
Date Received
December 15, 1987
Decision Date
February 18, 1988
Product Code
GEC
Advisory Committee
General, Plastic Surgery
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
GEC Brush, Scrub, Operating-Room

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Other Clearances by Absorbent Cotton Co., Inc.

K Number Device Name
K883250 STERI-CLENS WOUND CARE KIT
K880613 ACCO(R) FACE MASK
K874741 STERI-CLENS(TM) SURGICAL SCRUB SPONGE
K873523 PLAIN DRY GAUZE
K854740 PRIMADERM
K850126 OIL EMULSION NON-ADHERING DRESSING
K844095 WET DRESSING WATER-STERILE
K844096 WET DRESSING SALINE-STERILE
K781727 CHANGE IN STERILIZATION PROCEDURE