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

FILTER, AIR, CUTTER MAINLINE

K Number: K770375 · Decision Mar 1, 1977
Classifications
1
FEI Numbers
143
Registration Numbers
143
Same Product Code
199
Applicant Total
39
Review Days
4

Basic Information

Device Name
FILTER, AIR, CUTTER MAINLINE
K Number
K770375
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5260
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
CUTTER LABORATORIES, INC.
Date Received
February 25, 1977
Decision Date
March 1, 1977
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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