Medical Device Manufacturer · US , Mchenry , IL

Spirometrics, Inc. - FDA 510(k) Cleared Devices

11 submissions · 11 cleared · Since 1983

Total

Cleared

Denied

Spirometrics, Inc. has 11 FDA 510(k) cleared anesthesiology devices. Based in Mchenry, US.

Historical record: 11 cleared submissions from 1983 to 1992.

Browse the complete list of FDA 510(k) cleared anesthesiology devices from this manufacturer. Filter by specialty or product code using the sidebar.

Spirometrics, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Spirometrics, Inc.

11 devices

1-11 of 11

Cleared Jul 27, 1992

PEAK FLOW MONITOR

K915059 · BZH

Anesthesiology · 262d

Cleared Jul 22, 1991

CMD/DLCO DIAGNOSTIC SPIROMETER

K911358 · BTY

Anesthesiology · 116d

SPIROMETRICS MODEL 2600 MIRO SPIROMETER

K901057 · BZG

Anesthesiology · 28d

Cleared Jan 19, 1989

SPIROMETRICS MODEL 2200 SM200 FLOW SENSOR

K884464 · JAX

Anesthesiology · 87d

Cleared Nov 09, 1988

SPIROMETRICS MODEL 2141 SPIRO-FILTER(TM)

K884465 · CAH

General Hospital · 16d

Cleared Jan 15, 1987

SPIROMETRICS MODEL 2500 FLOWMATE(TM)

K863953 · BZM

Anesthesiology · 97d

Cleared Feb 14, 1985

SPIROMETRICS 2453 & SMI III

K850045 · BTY

Anesthesiology · 38d

Cleared Nov 20, 1984

SPIROMETRICS 2451 & SMI I

K844333 · BZG

Anesthesiology · 13d

Cleared Jun 24, 1983

SPIROMETRICS BREON 2400 & SMI 2400

K831497 · BZG

Anesthesiology · 45d

Spirometrics, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Spirometrics, Inc.

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