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

CHANGE IN STERILIZATION PROCEDURE

K Number: K781727 · Decision Dec 4, 1978
Classifications
1
FEI Numbers
3
Registration Numbers
3
Same Product Code
0
Applicant Total
10
Review Days
54

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Basic Information

Device Name
CHANGE IN STERILIZATION PROCEDURE
K Number
K781727
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.3065
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
Absorbent Cotton Co., Inc.
Date Received
October 11, 1978
Decision Date
December 4, 1978
Product Code
GOY
Advisory Committee
Microbiology
Review Advisory Committee
CH
Third Party
N

Classifications

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

Product Code Device Name
GOY Antisera, Agglutinating, B. Pertussis, All

Other Clearances by Absorbent Cotton Co., Inc.

K Number Device Name
K883250 STERI-CLENS WOUND CARE KIT
K880613 ACCO(R) FACE MASK
K875129 STERI-CLENS
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