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

SARSTEDT NEEDLE PROTECTOR

K Number: K003382 · Decision Mar 30, 2001
Classifications
1
FEI Numbers
440
Registration Numbers
440
Same Product Code
687
Applicant Total
6
Review Days
150

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Basic Information

Device Name
SARSTEDT NEEDLE PROTECTOR
K Number
K003382
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5570
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Sarstedt, Inc.
Date Received
October 31, 2000
Decision Date
March 30, 2001
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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K913622 HEMOPLUS