Medical Device Manufacturer · US , Waukesha , WI

Bci Intl., Inc. - FDA 510(k) Cleared Devices

20 submissions · 20 cleared · Since 1994

Total

Cleared

Denied

Bci Intl., Inc. has 20 FDA 510(k) cleared anesthesiology devices. Based in Waukesha, US.

Historical record: 20 cleared submissions from 1994 to 1999.

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

Bci Intl., 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 - Bci Intl., Inc.

20 devices

1-12 of 20

Cleared Jun 09, 1999

CAPNOCHECK II, MODEL 8400

K991086 · CCK

Anesthesiology · 70d

Cleared Jun 09, 1999

3402 HANDHELD PULSE OXIMETER

K991410 · DQA

Anesthesiology · 48d

Cleared Mar 25, 1999

BCI MINI-TORR PLUS, MODEL 6004

K984618 · DXN

Cardiovascular · 86d

Cleared Jan 22, 1999

6004 NIBP MONITOR WITH TEMPERATURE

BCI 3401 HANDHELD PULSE OXIMETER

K980714 · DQA

Anesthesiology · 29d

Cleared Mar 11, 1998

REUSABLE FINGER SENSOR 3444

K974697 · DQH

Cardiovascular · 85d

Cleared Nov 12, 1997

BCI MODEL 6004 NIBP MONITOR (6004)

K970801 · DXN

Cardiovascular · 253d

Bci Intl., Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Bci Intl., Inc.

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