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.

Xanar, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

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

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

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