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

I.D.A. SYRINGES

K Number: K931632 · Decision Aug 24, 1993
Classifications
1
FEI Numbers
548
Registration Numbers
548
Same Product Code
747
Applicant Total
1
Review Days
144

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Basic Information

Device Name
I.D.A. SYRINGES
K Number
K931632
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5860
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Pt Hasoon Chandra
Date Received
April 2, 1993
Decision Date
August 24, 1993
Product Code
FMF
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
FMF Syringe, Piston

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