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

COUNTER, DISPOSABLE SURGICAL NEEDLE

K Number: K790039 · Decision Jan 17, 1979
Classifications
1
FEI Numbers
92
Registration Numbers
92
Same Product Code
112
Applicant Total
44
Review Days
9

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Basic Information

Device Name
COUNTER, DISPOSABLE SURGICAL NEEDLE
K Number
K790039
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5570
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Anago, Inc.
Date Received
January 8, 1979
Decision Date
January 17, 1979
Product Code
MMK
Advisory Committee
General Hospital
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
MMK Container, Sharps

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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
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