FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇱 Israel

BONE INJECTION GUN (B.I.G.) FOR PEDIATRICS, MODEL 1ST

K Number: K022415 · Decision Oct 11, 2002
Classifications
1
FEI Numbers
440
Registration Numbers
440
Same Product Code
687
Applicant Total
7
Review Days
79

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Basic Information

Device Name
BONE INJECTION GUN (B.I.G.) FOR PEDIATRICS, MODEL 1ST
K Number
K022415
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5570
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Waismed, Ltd.
Date Received
July 24, 2002
Decision Date
October 11, 2002
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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Other Clearances by Waismed, Ltd.

K Number Device Name
K211968 NIO+ Adult
K190538 NIO-I
K160805 NIO-P
K142086 NIO -INTRAOSSEOUS DEVICE
K062940 BONE INJECTION GUN (B.I.G.)
K981853 BONE INJECTION GUN (B.I.G.) DEVICE