# Konigsberg Instruments, Inc.

- Location (FDA's records): Walker, MI
- FDA decisions: 3 (1981–1998): 3 510(k) clearances
- Product codes: LIT (1), FFX (1), FFT (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
- K980980: Motility Probe Model Numbers P31 Thru P38, P40 Thru P43 and P50 (Jun 15, 1998)
- K813331: P51 Angioplasty Pressure Transducer (Dec 29, 1981)
- K811083: Esophageal Motility Probe (Aug 13, 1981)

Source page: https://510kreport.com/company/konigsberg-instruments