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

IO Needle Safety Sheath

K Number: K220890 · Decision Oct 31, 2022
Classifications
1
FEI Numbers
440
Registration Numbers
440
Same Product Code
687
Applicant Total
10
Review Days
217

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Basic Information

Device Name
IO Needle Safety Sheath
K Number
K220890
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5570
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Actuated Medical, Inc.
Date Received
March 28, 2022
Decision Date
October 31, 2022
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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