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

BKMI DISPOSABLE SYRINGE

K Number: K971487 · Decision Sep 4, 1997
Classifications
1
FEI Numbers
440
Registration Numbers
440
Same Product Code
687
Applicant Total
1
Review Days
134

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Basic Information

Device Name
BKMI DISPOSABLE SYRINGE
K Number
K971487
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5570
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Sumi Salud C.A.
Date Received
April 23, 1997
Decision Date
September 4, 1997
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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