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

MEDIPART DISPOSABLE AEROSOL SYSTEM MP-070-PTD

K Number: K894138 · Decision Sep 26, 1989
Classifications
1
FEI Numbers
189
Registration Numbers
189
Same Product Code
507
Applicant Total
49
Review Days
105

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Basic Information

Device Name
MEDIPART DISPOSABLE AEROSOL SYSTEM MP-070-PTD
K Number
K894138
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5630
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Medipart Jerry Alexander
Date Received
June 13, 1989
Decision Date
September 26, 1989
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 Medipart Jerry Alexander

K Number Device Name
K896885 DISPOSABLE RESPIRTORY KIT (MP-200)
K896125 MEDIPART DISPOSABLE XENON-133 REBREATHING MP-0133M
K896124 MEDIPART DISPOSABLE XENON-133 REBREATHING MP-0133
K896475 DISP. RADIOAEROSOL KIT (MP-400) TO FIT LEAD SHIELD
K896476 DISP. RADIOAEROSOL KIT (MP-400-M) TO FIT SHIELD
K893532 RESUBMITTED RADIOAEROSOL CONT. SYSTEM MP-963
K862786 MP-50T DISPOSABLE BREATHING CIRCUIT FILTER
K862795 MP-070-M RADIOAEROSOL KIT
K862791 MP-30XM-IE FACE MASK AND FILTER KIT
K862783 MP-XMV DISPOSABLE FACE MASK
Search all 49 clearances from Medipart Jerry Alexander →