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Xanar, Inc.

Colorado Springs, CO, US

Xanar, Inc. appears in FDA device records in Colorado Springs, CO. FDA records list 11 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.

FDA records held for this company

510(k) clearances
11
PMA records
0
Recall records
0
Registered establishments
0

510(k) clearance history

FDA records hold 11 510(k) clearances for Xanar, Inc. between 1983 and 1986. The busiest year on record is 1985, with 4. The most recent is 1986, with 4.

Clearances by year, as a table
510(k) clearance decisions for Xanar, Inc., by decision year
YearClearances
19832
19841
19854
19864
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K861688XANAR CO2 SURGICAL LASER SYSTEM MODEL XAP-15GEXSubstantially Equivalent
K852436AMBULASEGEXSubstantially Equivalent
K860496MODEL NY-110 FOR UPPER & LOWER (GU) & PULMONARYLNKSubstantially Equivalent
K853620MODEL XA-50 - CO2 SURGICAL LASERGEXSubstantially Equivalent
K850818CO 2 SURGICAL LASER SYSTEM NA-120GEXSubstantially Equivalent
K850805CO 2 SURGICAL LASER SYSTEM MODEL NA-40GEXSubstantially Equivalent
K850804CO 2 SURGICAL LASER SYSTEM NA-30GEXSubstantially Equivalent
K844087XANAR MODEL XSE-300 SMOKE EVACULATERFYDSubstantially Equivalent
K841860CO2 SURGICAL LASER SYSTEM XML-10EWGSubstantially Equivalent
K837224UNKNOWNSubstantially Equivalent
K837216MODEL XA-15 LASER SYSTEM FOR SURGERYSubstantially Equivalent

Registered establishments

No FDA establishment registrations recorded against this company.

FDA product codes

Recall records

No recall records for this company in the ingested FDA data.

Verification record

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Data as of , FDA export datePage updated Source: openFDA, public domain