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

MONOJECT STERILE 1/2 CC & 1CC SYRINGES W & W/O NEE

K Number: K851090 · Decision Apr 12, 1985
Classifications
1
FEI Numbers
553
Registration Numbers
553
Same Product Code
738
Applicant Total
191
Review Days
25

Basic Information

Device Name
MONOJECT STERILE 1/2 CC & 1CC SYRINGES W & W/O NEE
K Number
K851090
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5860
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
SHERWOOD MEDICAL CO.
Date Received
March 18, 1985
Decision Date
April 12, 1985
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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