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

MEDICAL DEPOT NEBULIZER, MODEL POWER NEB 2

K Number: K003344 · Decision Mar 15, 2001
Classifications
1
FEI Numbers
189
Registration Numbers
189
Same Product Code
507
Applicant Total
3
Review Days
141

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Basic Information

Device Name
MEDICAL DEPOT NEBULIZER, MODEL POWER NEB 2
K Number
K003344
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5630
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Medical Depot, Inc.
Date Received
October 25, 2000
Decision Date
March 15, 2001
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)

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (CAF), ordered by most recent decision date.

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Other Clearances by Medical Depot, Inc.

K Number Device Name
K012006 MEDICAL DEPOT POWER NEB 1
K003783 MEDICAL DEPOT-WHEELCHAIRS, MODEL SENTRA,ASTAIRE AND VIPER