Xanar, Inc.
Xanar, Inc. appears in FDA public data with 0 recalls, 12 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on October 3, 1986.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 12
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K861688 | XANAR CO2 SURGICAL LASER SYSTEM MODEL XAP-15 | October 3, 1986 |
| K852436 | AMBULASE | April 18, 1986 |
| K860496 | MODEL NY-110 FOR UPPER & LOWER (GU) & PULMONARY | March 14, 1986 |
| K853620 | MODEL XA-50 - CO2 SURGICAL LASER | January 24, 1986 |
| K850805 | CO 2 SURGICAL LASER SYSTEM MODEL NA-40 | August 15, 1985 |
| K850818 | CO 2 SURGICAL LASER SYSTEM NA-120 | August 15, 1985 |
| K850804 | CO 2 SURGICAL LASER SYSTEM NA-30 | August 15, 1985 |
| K844087 | XANAR MODEL XSE-300 SMOKE EVACULATER | February 27, 1985 |
| K841860 | CO2 SURGICAL LASER SYSTEM XML-10 | November 8, 1984 |
| K833325 | AMBULASE XAM-15 XANAR SURG. LASER | January 26, 1984 |
| K837224 | UNKNOWN | May 2, 1983 |
| K837216 | MODEL XA-15 LASER SYSTEM FOR SURGERY | April 4, 1983 |