ClearanceBrief
Company ยท DK

Biometer Intl. A/S

FDA 510(k) clearances and medical device recalls filed under this name, 1986 to 1993. Name variants (Inc, Corp, punctuation) are merged.

9510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
BXNStimulator, Nerve, Battery-Powered6
IPFStimulator, Muscle, Powered2
KOIStimulator, Nerve, Peripheral, Electric1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Sep 1, 1993K925159TOF-GUARD TRANSMISSION MONITOR
Biometer Intl. A/S, DK
KOI
May 28, 1992K914231ELPHA 2000
Biometer Intl. A/S, DK
IPF
Oct 3, 1989K892396MINI ACCELOGRAPH NEUROMUSCULAR TRANS. MONITOR
Biometer Intl. A/S, DK
BXN
Jul 28, 1989K893485ACCELOGRAPH NEUROMUSCULAR TRANSMISSION MONITOR
Biometer Intl. A/S, DK
BXN
Jul 14, 1989K890746MYOTEST DBS NERVE STIMULATOR
Biometer Intl. A/S, DK
BXN
Jun 16, 1989K881196AM 706 ELECTROMYOGRAPH, STIM., NEURO., EXTERNAL
Biometer Intl. A/S, DK
IPF
Mar 16, 1987K870619ACCELOGRAPH
Biometer Intl. A/S, DK
BXN
Mar 20, 1986K860187MYOGRAPH 2000 - NEURO. TRANS. MONITOR & RECORDING
Biometer Intl. A/S, DK
BXN
Mar 20, 1986K860186MYOTEST - NERVE STIMULATOR
Biometer Intl. A/S, DK
BXN

Latest recalls

DateFirm and productCodeLinked 510(k)
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