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

FILTER

K Number: K970102 · Decision Jun 24, 1997
Classifications
1
FEI Numbers
141
Registration Numbers
141
Same Product Code
201
Applicant Total
16
Review Days
162

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Basic Information

Device Name
FILTER
K Number
K970102
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5260
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Promedic, Inc.
Date Received
January 13, 1997
Decision Date
June 24, 1997
Product Code
CAH
Advisory Committee
Anesthesiology
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
CAH Filter, Bacterial, Breathing-Circuit

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Other Clearances by Promedic, Inc.

K Number Device Name
K131889 EUM 100PRO
K112318 CLEARPATH 24
K072756 NON-IV ADAPTER FOR INFANT NG TUBE
K060497 BABYAIR
K060842 REVJET TURBO
K052903 PEDIATRIC FEEDING TUBE
K031409 URINARY CATHETERS
K024190 FENESTRATED INFUSION CATHETER
K023579 GAS SAMPLING LINES
K020005 INFANT FEEDING TUBES
Search all 16 clearances from Promedic, Inc. →