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Xanar, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
12
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K861688XANAR CO2 SURGICAL LASER SYSTEM MODEL XAP-15October 3, 1986
K852436AMBULASEApril 18, 1986
K860496MODEL NY-110 FOR UPPER & LOWER (GU) & PULMONARYMarch 14, 1986
K853620MODEL XA-50 - CO2 SURGICAL LASERJanuary 24, 1986
K850818CO 2 SURGICAL LASER SYSTEM NA-120August 15, 1985
K850805CO 2 SURGICAL LASER SYSTEM MODEL NA-40August 15, 1985
K850804CO 2 SURGICAL LASER SYSTEM NA-30August 15, 1985
K844087XANAR MODEL XSE-300 SMOKE EVACULATERFebruary 27, 1985
K841860CO2 SURGICAL LASER SYSTEM XML-10November 8, 1984
K833325AMBULASE XAM-15 XANAR SURG. LASERJanuary 26, 1984
K837224UNKNOWNMay 2, 1983
K837216MODEL XA-15 LASER SYSTEM FOR SURGERYApril 4, 1983