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

OXY-DIAL

K Number: K852618 · Decision Sep 18, 1985
Classifications
1
FEI Numbers
95
Registration Numbers
95
Same Product Code
18
Applicant Total
12
Review Days
90

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Basic Information

Device Name
OXY-DIAL
K Number
K852618
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
868.5600
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Ashai Co. , Ltd.
Date Received
June 20, 1985
Decision Date
September 18, 1985
Product Code
BYF
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
BYF Mask, Oxygen, Low Concentration, Venturi

Similar 510(k) Clearances

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

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Other Clearances by Ashai Co. , Ltd.

K Number Device Name
K870428 AEROSOL ONE, NEBULIZER PUMP
K852622 AEROSOL ONE
K852620 SAFE.N.SURE
K852627 MAXI-NEB
K852628 NASAL ONE
K852625 OXY-TUBE
K852629 AERO-MASK TWO
K852624 OXY-TWO
K852626 AERO-MASK ONE
K852623 OXY-ONE
Search all 12 clearances from Ashai Co. , Ltd. →