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

SAFEPRO SAFETY SYRINGE

K Number: K022063 · Decision Aug 29, 2002
Classifications
1
FEI Numbers
130
Registration Numbers
130
Same Product Code
161
Applicant Total
3
Review Days
65

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Basic Information

Device Name
SAFEPRO SAFETY SYRINGE
K Number
K022063
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5860
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Formosa Medical Devices, Inc.
Date Received
June 25, 2002
Decision Date
August 29, 2002
Product Code
MEG
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
MEG Syringe, Antistick

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (MEG), ordered by most recent decision date.

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Other Clearances by Formosa Medical Devices, Inc.

K Number Device Name
K050134 ICC INSULIN SAFEPRO SAFETY SYRINGE
K031830 SAFEPRO PLUS SAFETY SYRINGE