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

PLAIN DRY GAUZE

K Number: K873523 · Decision Oct 9, 1987
Classifications
1
FEI Numbers
59
Registration Numbers
59
Same Product Code
270
Applicant Total
10
Review Days
38

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Basic Information

Device Name
PLAIN DRY GAUZE
K Number
K873523
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Applicant
Absorbent Cotton Co., Inc.
Date Received
September 1, 1987
Decision Date
October 9, 1987
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 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
K854740 PRIMADERM
K850126 OIL EMULSION NON-ADHERING DRESSING
K844095 WET DRESSING WATER-STERILE
K844096 WET DRESSING SALINE-STERILE
K781727 CHANGE IN STERILIZATION PROCEDURE