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

ANAGO STERILE PRODUCTS; STOCKINETTES

K Number: K813097 · Decision Mar 10, 1982
Classifications
1
FEI Numbers
200
Registration Numbers
200
Same Product Code
449
Applicant Total
44
Review Days
127

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Basic Information

Device Name
ANAGO STERILE PRODUCTS; STOCKINETTES
K Number
K813097
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4370
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Anago, Inc.
Date Received
November 3, 1981
Decision Date
March 10, 1982
Product Code
KKX
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
KKX Drape, Surgical, Antimicrobial

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Other Clearances by Anago, Inc.

K Number Device Name
K925659 U.C.E.Z. LENS CLEANER KIT
K930161 ANAGO SPINAL ANESTHESIA TRAY
K926589 ANAGO WARM PACK
K926590 ANAGO DISPOSABLE INSTANT COLD PACK
K926137 ANAGO FEM-COOL/FEM-COOL PETITE
K920615 ANAGO CONTINUOUS EPIDURAL ANESTHESIA TRAY/KIT
K915415 GUARDALL SHIELD
K913558 RELIABLE CONE STYLE FACE MASK
K905865 ANTI-FOR SURGICAL FACE MASK
K905749 SURGICAL FACE MASK
Search all 44 clearances from Anago, Inc. →