Medical Device Manufacturer · US , Auburn , ME

Micro Direct, Inc. - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 1994

Total

Cleared

Denied

Micro Direct, Inc. has 9 FDA 510(k) cleared medical devices. Based in Auburn, US.

Historical record: 9 cleared submissions from 1994 to 2004. Primary specialty: Anesthesiology.

Browse the FDA 510(k) cleared devices submitted by Micro Direct, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Micro Direct, Inc.

9 devices

1-9 of 9

Cleared May 19, 2004

MICRO H2 BREATH MONITORING DEVICE WITH HYDRA SOFTWARE UTILITY

Anesthesiology · 238d

Cleared Aug 27, 2003

MICROPEAK

K030586 · BZH

Anesthesiology · 184d

Cleared Nov 21, 1997

SPIROSAFE FILTER

K973314 · CAH

General Hospital · 79d

Cleared Jun 17, 1997

MICRODL DIARYCARD SPIROMETER

K965042 · BZG

Anesthesiology · 182d

Anesthesiology · 638d

Cleared Nov 21, 1994

MICRO MPM

K940375 · CAP

Anesthesiology · 299d

Micro Direct, Inc. - FDA 510(k) Cleared Devices

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