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

SHARPS CONTAINER 18 GALLON

K Number: K944121 · Decision Jan 27, 1995
Classifications
1
FEI Numbers
440
Registration Numbers
440
Same Product Code
687
Applicant Total
13
Review Days
157

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Basic Information

Device Name
SHARPS CONTAINER 18 GALLON
K Number
K944121
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5570
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Bci, Inc.
Date Received
August 23, 1994
Decision Date
January 27, 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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