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

FLOW-EZE BLUNT CANNULA (1999BC)

K Number: K972538 · Decision Jul 15, 1998
Classifications
1
FEI Numbers
440
Registration Numbers
440
Same Product Code
687
Applicant Total
17
Review Days
372

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Basic Information

Device Name
FLOW-EZE BLUNT CANNULA (1999BC)
K Number
K972538
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5570
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Acacia, Inc.
Date Received
July 8, 1997
Decision Date
July 15, 1998
Product Code
FMI
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
FMI Needle, Hypodermic, Single Lumen

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