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

MICROLAB SPIROMETER

K Number: K031102 · Decision Dec 1, 2003
Classifications
1
FEI Numbers
92
Registration Numbers
92
Same Product Code
227
Applicant Total
9
Review Days
238

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Basic Information

Device Name
MICROLAB SPIROMETER
K Number
K031102
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.1840
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Micro Direct, Inc.
Date Received
April 7, 2003
Decision Date
December 1, 2003
Product Code
BZG
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
BZG Spirometer, Diagnostic

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Other Clearances by Micro Direct, Inc.

K Number Device Name
K033688 MICRO H2 BREATH MONITORING DEVICE WITH HYDRA SOFTWARE UTILITY
K030586 MICROPEAK
K973314 SPIROSAFE FILTER
K965042 MICRODL DIARYCARD SPIROMETER
K963376 MICRO H2
K963035 MICRO SPIROMETER
K950197 MICROCO
K940375 MICRO MPM