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

CHEST BELLOWS, SMALL

K Number: K772367 · Decision Jan 11, 1978
Classifications
1
FEI Numbers
2
Registration Numbers
2
Same Product Code
10
Applicant Total
69
Review Days
15

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Basic Information

Device Name
CHEST BELLOWS, SMALL
K Number
K772367
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.1750
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Honeywell, Inc.
Date Received
December 27, 1977
Decision Date
January 11, 1978
Product Code
CCM
Advisory Committee
Anesthesiology
Review Advisory Committee
AN
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
CCM Plethysmograph, Pressure

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