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

PEAK EXPIRATORY FLOW METER

K Number: K912866 · Decision Aug 13, 1992
Classifications
1
FEI Numbers
41
Registration Numbers
41
Same Product Code
79
Applicant Total
13
Review Days
412

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Basic Information

Device Name
PEAK EXPIRATORY FLOW METER
K Number
K912866
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.1860
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Health Products, Inc.
Date Received
June 28, 1991
Decision Date
August 13, 1992
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 Health Products, Inc.

K Number Device Name
K912943 THRESHOLD 2X INSPIRATORY MUSCLE TRAINER
K911807 METERED DOSE INHALER (MDI) SPACER
K902292 MODIFIED ASSESS(R) PEAK FLOW METER
K896953 MODIFIED ASSESS(R) PEAK FLOW METER
K894353 ORTHODERM CONVERTIBLE
K890426 CONSUMMATE AIR THERAPY BED
K874801 ORTHODERM THERAPY BED
K871742 MODIFIED USE OF PLEX INSPIRATORY MUSCLE TRAINER
K870514 THRESHOLD(TM) INSPIRATORY MUSCLE TRAINER
K864719 PFLEX EM(TM) (EXERCISE MONITOR)
Search all 13 clearances from Health Products, Inc. →