# Biometer Intl. A/S

- Location (FDA's records): Denmark, DK
- FDA decisions: 9 (1986–1993): 9 510(k) clearances
- Product codes: BXN (6), IPF (2), KOI (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K925159: Tof-Guard Transmission Monitor (Sep 1, 1993)
- K914231: ELPHA 2000 (May 28, 1992)
- K892396: Mini Accelograph Neuromuscular Trans. Monitor (Oct 3, 1989)
- K893485: Accelograph Neuromuscular Transmission Monitor (Jul 28, 1989)
- K890746: Myotest DBS Nerve Stimulator (Jul 14, 1989)
- K881196: AM 706 Electromyograph, Stim., Neuro., External (Jun 16, 1989)
- K870619: Accelograph (Mar 16, 1987)
- K860187: Myograph 2000 - Neuro. Trans. Monitor & Recording (Mar 20, 1986)

Source page: https://510kreport.com/company/biometer-intl-a-s