# Laser Spectrum, Inc.

- Location (FDA's records): Chicago, IL
- FDA decisions: 5 (1984–1986): 5 510(k) clearances
- Product codes: HHR (1), GEX (1), HET (1), EWQ (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
- K863520: CO2 Laser Micromanipulator (Oct 6, 1986)
- K844765: Accessory Set for CO2 Laser Bronchoscopy Instrumen (Apr 8, 1985)
- K841781: Model 305AA Portable Laser (Nov 7, 1984)
- K842498: Daniell DBL Puncture Laser Laparoscopy (Sep 25, 1984)
- K841668: CO2 Laparoscope (Apr 23, 1984)

Source page: https://510kreport.com/company/laser-spectrum
