FDA 510(k) FDA class 1 Substantially Equivalent 🇦🇺 Australia

MAXI-NEB

K Number: K852627 · Decision Sep 26, 1985
Classifications
1
FEI Numbers
140
Registration Numbers
140
Same Product Code
61
Applicant Total
12
Review Days
98

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
MAXI-NEB
K Number
K852627
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
868.5640
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Ashai Co. , Ltd.
Date Received
June 20, 1985
Decision Date
September 26, 1985
Product Code
CCQ
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
CCQ Nebulizer, Medicinal, Non-Ventilatory (Atomizer)

Similar 510(k) Clearances

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

View all

Other Clearances by Ashai Co. , Ltd.

K Number Device Name
K870428 AEROSOL ONE, NEBULIZER PUMP
K852622 AEROSOL ONE
K852620 SAFE.N.SURE
K852628 NASAL ONE
K852625 OXY-TUBE
K852629 AERO-MASK TWO
K852624 OXY-TWO
K852618 OXY-DIAL
K852626 AERO-MASK ONE
K852623 OXY-ONE
Search all 12 clearances from Ashai Co. , Ltd. →