Laser Spectrum, Inc.
Laser Spectrum, Inc. appears in FDA public data with 0 recalls, 5 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on October 6, 1986.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 5
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K863520 | CO2 LASER MICROMANIPULATOR | October 6, 1986 |
| K844765 | ACCESSORY SET FOR CO2 LASER BRONCHOSCOPY INSTRUMEN | April 8, 1985 |
| K841781 | MODEL 305AA PORTABLE LASER | November 7, 1984 |
| K842498 | DANIELL DBL PUNCTURE LASER LAPAROSCOPY | September 25, 1984 |
| K841668 | CO2 LAPAROSCOPE | April 23, 1984 |