Lares Manufacturing Co., Inc.
Lares Manufacturing Co., Inc. appears in FDA public data with 0 recalls, 6 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on November 14, 1983.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 6
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K831351 | PERMALUX VISIBLE CURE COMPOSITE RESTOR | November 14, 1983 |
| K801535 | LARES HANDPIECE OIL | December 16, 1980 |
| K801592 | FIBER OPTIC HOSE | July 21, 1980 |
| K801591 | FIBER OPTIC ILLUMINATOR | July 21, 1980 |
| K801534 | LARES AIR PRESSURE GAUGE | July 14, 1980 |
| K780038 | DENTAL HANDPIECE | January 20, 1978 |