Medical Device Manufacturer · US , Cleveland , TN

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

19 submissions · 19 cleared · Since 1994

Recent clearances: PRIMA VENTILATOR HOSES, PRIMA BREATHING BAGS, PRIMA CUSTOM ANESTESIA CIRCUIT

Total

Cleared

Denied

Prima, Inc. has 19 FDA 510(k) cleared anesthesiology devices. Based in Cleveland, US.

Historical record: 19 cleared submissions from 1994 to 1995.

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

Prima, Inc. is one of 5795 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

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

19 devices

1-12 of 19

Cleared May 22, 1995

PRIMA VENTILATOR HOSES

PRIMA CUSTOM ANESTESIA CIRCUIT

PRIMA ADULT TEMPERATURE MONITORING ANESTHESIA CIRCUITS

General Hospital · 24d

Cleared May 22, 1995

PRIMA PEDIATRIC GAS SAMPLING CIRCUITS

K952016 · CAI

Anesthesiology · 24d

Cleared May 22, 1995

PRIMA MAPLESON D CIRCUIT

K952017 · CAI

Anesthesiology · 24d

Cleared May 22, 1995

PRIMA COAXIAL CIRCUITS

K952018 · CAI

Anesthesiology · 24d

Cleared May 22, 1995

PRIMA ADULT GAS SAMPLING CIRCUITS

K952019 · CAI

Anesthesiology · 24d

Cleared May 22, 1995

PRIMA PEDIATRIC ANESTHESIA CIRCUITS

K952020 · CAI

Anesthesiology · 24d

Cleared May 22, 1995

PRIMA HYUPERINFLATION SYSTEM

K952021 · BZR

Anesthesiology · 24d

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

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

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