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

SAFETYGLIDE NEEDLE

K Number: K951254 · Decision Oct 7, 1995
Classifications
1
FEI Numbers
466
Registration Numbers
466
Same Product Code
680
Applicant Total
632
Review Days
200

Basic Information

Device Name
SAFETYGLIDE NEEDLE
K Number
K951254
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5570
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
BD BECTON DICKINSON VACUTAINER SYSTEMS PREANALYTIC
Date Received
March 21, 1995
Decision Date
October 7, 1995
Product Code
FMI
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
FMI Needle, Hypodermic, Single Lumen

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