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

PEAK FLOW MONITOR

K Number: K813414 · Decision Dec 31, 1981
Classifications
1
FEI Numbers
41
Registration Numbers
41
Same Product Code
79
Applicant Total
6
Review Days
24

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Basic Information

Device Name
PEAK FLOW MONITOR
K Number
K813414
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.1860
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Biotrine Corp.
Date Received
December 7, 1981
Decision Date
December 31, 1981
Product Code
BZH
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
BZH Meter, Peak Flow, Spirometry

Similar 510(k) Clearances

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

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Other Clearances by Biotrine Corp.

K Number Device Name
K915060 ASTECH HOME PEAK FLOW METER
K883704 MULTIICHALLENGE NEBULIZER SYSTEM
K863134 MULTISPIRO SA/100
K844226 B-1000
K812825 FLO-COR I