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

ICEL ULTRASONIC NEBULIZER MODELS PU 12000 AIR AND PU 12300 AIR

K Number: K972371 · Decision Aug 19, 1997
Classifications
1
FEI Numbers
189
Registration Numbers
189
Same Product Code
507
Applicant Total
2
Review Days
55

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Basic Information

Device Name
ICEL ULTRASONIC NEBULIZER MODELS PU 12000 AIR AND PU 12300 AIR
K Number
K972371
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5630
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Brasamerica Medical Equipment, Inc.
Date Received
June 25, 1997
Decision Date
August 19, 1997
Product Code
CAF
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
CAF Nebulizer (Direct Patient Interface)

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Other Clearances by Brasamerica Medical Equipment, Inc.

K Number Device Name
K983736 ICEL EVOLUSONIC PORTABLE ULTRASONIC NEBULIZER