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

NIO -INTRAOSSEOUS DEVICE

K Number: K142086 · Decision Aug 28, 2014
Classifications
1
FEI Numbers
440
Registration Numbers
440
Same Product Code
687
Applicant Total
7
Review Days
28

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Basic Information

Device Name
NIO -INTRAOSSEOUS DEVICE
K Number
K142086
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
880.5570
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Waismed, Ltd.
Date Received
July 31, 2014
Decision Date
August 28, 2014
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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K211968 NIO+ Adult
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K022415 BONE INJECTION GUN (B.I.G.) FOR PEDIATRICS, MODEL 1ST
K981853 BONE INJECTION GUN (B.I.G.) DEVICE