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

MONOJECT MAGELLAN INSULIN AND TUBERCULIN SAFETY SYRINGE

K Number: K061492 · Decision Aug 3, 2006
Classifications
1
FEI Numbers
553
Registration Numbers
553
Same Product Code
738
Applicant Total
14
Review Days
64

Basic Information

Device Name
MONOJECT MAGELLAN INSULIN AND TUBERCULIN SAFETY SYRINGE
K Number
K061492
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5860
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
TYCO HEALTHCARE
Date Received
May 31, 2006
Decision Date
August 3, 2006
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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