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

UNIVEC NONREUSABLE LOCKING SYRINGE

K Number: K951619 · Decision Jun 6, 1995
Classifications
1
FEI Numbers
548
Registration Numbers
548
Same Product Code
747
Applicant Total
7
Review Days
71

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Basic Information

Device Name
UNIVEC NONREUSABLE LOCKING SYRINGE
K Number
K951619
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5860
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Univec, Inc.
Date Received
March 27, 1995
Decision Date
June 6, 1995
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

Similar 510(k) Clearances

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

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Other Clearances by Univec, Inc.

K Number Device Name
K020500 UNIVEC BIFURCATED SLIDING SHEATH SYRINGE
K993996 UNIVEC AUTO-DISABLE HYPODERMIC SYRINGE
K000747 UNIVEC TWO PIECE SYRINGE
K961877 PISTON SYRINGE
K933469 UNIVEC NON-REUSABLE SYRINGE
K943679 UNIVEC NONRESUSABLE LOCKING SYRINGE