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

CMD/DLCO DIAGNOSTIC SPIROMETER

K Number: K911358 · Decision Jul 22, 1991
Classifications
1
FEI Numbers
17
Registration Numbers
17
Same Product Code
62
Applicant Total
11
Review Days
116

Basic Information

Device Name
CMD/DLCO DIAGNOSTIC SPIROMETER
K Number
K911358
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.1890
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
SPIROMETRICS, INC.
Date Received
March 28, 1991
Decision Date
July 22, 1991
Product Code
BTY
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
BTY Calculator, Predicted Values, Pulmonary Function

Similar 510(k) Clearances

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Other Clearances by SPIROMETRICS, INC.

K Number Device Name
K915059 PEAK FLOW MONITOR
K900322 CO/CMD-1
K901057 SPIROMETRICS MODEL 2600 MIRO SPIROMETER
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. →