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

SPIROMETRICS MODEL 2600 MIRO SPIROMETER

K Number: K901057 · Decision Apr 3, 1990
Classifications
1
FEI Numbers
92
Registration Numbers
92
Same Product Code
227
Applicant Total
11
Review Days
28

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Basic Information

Device Name
SPIROMETRICS MODEL 2600 MIRO SPIROMETER
K Number
K901057
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.1840
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Spirometrics, Inc.
Date Received
March 6, 1990
Decision Date
April 3, 1990
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

Similar 510(k) Clearances

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

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Other Clearances by Spirometrics, Inc.

K Number Device Name
K915059 PEAK FLOW MONITOR
K911358 CMD/DLCO DIAGNOSTIC SPIROMETER
K900322 CO/CMD-1
K900673 SERIAL FLOW
K884464 SPIROMETRICS MODEL 2200 SM200 FLOW SENSOR
K884465 SPIROMETRICS MODEL 2141 SPIRO-FILTER(TM)
K863953 SPIROMETRICS MODEL 2500 FLOWMATE(TM)
K850045 SPIROMETRICS 2453 & SMI III
K844333 SPIROMETRICS 2451 & SMI I
K831497 SPIROMETRICS BREON 2400 & SMI 2400
Search all 11 clearances from Spirometrics, Inc. →