Medical Device Manufacturer · DK , Denmark

Biometer Intl. A/S - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 1986

Total

Cleared

Denied

Biometer Intl. A/S has 9 FDA 510(k) cleared medical devices. Based in Denmark, DK.

Historical record: 9 cleared submissions from 1986 to 1993. Primary specialty: Anesthesiology.

Browse the FDA 510(k) cleared devices submitted by Biometer Intl. A/S Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Biometer Intl. A/S

9 devices

1-9 of 9

Cleared Sep 01, 1993

TOF-GUARD TRANSMISSION MONITOR

K925159 · KOI

Anesthesiology · 323d

Cleared May 28, 1992

ELPHA 2000

K914231 · IPF

Physical Medicine · 251d

Cleared Oct 03, 1989

MINI ACCELOGRAPH NEUROMUSCULAR TRANS. MONITOR

K892396 · BXN

Anesthesiology · 179d

Cleared Jul 28, 1989

ACCELOGRAPH NEUROMUSCULAR TRANSMISSION MONITOR

K893485 · BXN

Anesthesiology · 85d

Cleared Jul 14, 1989

MYOTEST DBS NERVE STIMULATOR

K890746 · BXN

Anesthesiology · 151d

Cleared Jun 16, 1989

AM 706 ELECTROMYOGRAPH, STIM., NEURO., EXTERNAL

K881196 · IPF

Physical Medicine · 452d

MYOTEST - NERVE STIMULATOR

K860186 · BXN

Anesthesiology · 57d

Cleared Mar 20, 1986

MYOGRAPH 2000 - NEURO. TRANS. MONITOR & RECORDING

K860187 · BXN

Anesthesiology · 57d

Biometer Intl. A/S - FDA 510(k) Cleared Devices

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