Medical Device Manufacturer · US , Walker , MI

Xanar, Inc. - FDA 510(k) Cleared Devices

12 submissions · 12 cleared · Since 1983

Total

Cleared

Denied

Xanar, Inc. has 12 FDA 510(k) cleared medical devices. Based in Walker, US.

Historical record: 12 cleared submissions from 1983 to 1986. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Xanar, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Xanar, Inc.

12 devices

1-12 of 12

Cleared Oct 03, 1986

XANAR CO2 SURGICAL LASER SYSTEM MODEL XAP-15

K861688 · GEX

General & Plastic Surgery · 154d

Cleared Apr 18, 1986

AMBULASE

K852436 · GEX

General & Plastic Surgery · 312d

Cleared Mar 14, 1986

MODEL NY-110 FOR UPPER & LOWER (GU) & PULMONARY

K860496 · LNK

Gastroenterology & Urology · 32d

Cleared Jan 24, 1986

MODEL XA-50 - CO2 SURGICAL LASER

K853620 · GEX

General & Plastic Surgery · 148d

Cleared Aug 15, 1985

CO 2 SURGICAL LASER SYSTEM NA-30

K850804 · GEX

General & Plastic Surgery · 169d

Cleared Aug 15, 1985

CO 2 SURGICAL LASER SYSTEM MODEL NA-40

K850805 · GEX

General & Plastic Surgery · 169d

Cleared Aug 15, 1985

CO 2 SURGICAL LASER SYSTEM NA-120

K850818 · GEX

General & Plastic Surgery · 168d

Cleared Feb 27, 1985

XANAR MODEL XSE-300 SMOKE EVACULATER

K844087 · FYD

General Hospital · 128d

Cleared Nov 08, 1984

CO2 SURGICAL LASER SYSTEM XML-10

K841860 · EWG

Ear, Nose, Throat · 188d

Cleared Jan 26, 1984

AMBULASE XAM-15 XANAR SURG. LASER

K833325

General & Plastic Surgery · 121d

MODEL XA-15 LASER SYSTEM FOR SURGERY

K837216

Radiology · 35d

Xanar, Inc. - FDA 510(k) Cleared Devices

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