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

UNITOX BOTOX SYRINGE

K Number: K123710 · Decision May 9, 2013
Classifications
1
FEI Numbers
548
Registration Numbers
548
Same Product Code
747
Applicant Total
10
Review Days
156

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Basic Information

Device Name
UNITOX BOTOX SYRINGE
K Number
K123710
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5860
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Bio-Med USA, Inc.
Date Received
December 4, 2012
Decision Date
May 9, 2013
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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