Medical Device Manufacturer · US , Washington , DC

Xanmed Corp. - FDA 510(k) Cleared Devices

9 submissions · 8 cleared · Since 1984

Total

Cleared

Denied

Xanmed Corp. has 8 FDA 510(k) cleared medical devices. Based in Washington, US.

Historical record: 8 cleared submissions from 1984 to 1987.

Browse the FDA 510(k) cleared devices submitted by Xanmed Corp. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Xanmed Corp.

9 devices

1-9 of 9

Cleared Jan 14, 1987

OBSTETRICAL/GYNECOLOGICAL CUSTOM SURGICAL KIT

K864623 · KNA

Obstetrics & Gynecology · 50d

Cleared Aug 21, 1985

ORTHOPEDIC CUSTOM SURGICAL KIT

K844595 · LXH

Orthopedic · 268d

Cleared Aug 01, 1985

EMERGENCY ROOM & MINOR OFFICE PROCEDURE CUSTOM KIT

K844596

General & Plastic Surgery · 248d

Cleared Jun 21, 1985

CARDIOVASCULAR CUSTOM SURGICAL KIT

K844593 · DYB

Cardiovascular · 207d

Cleared Jun 13, 1985

NEURO CUSTOM SURGICAL KIT

General & Plastic Surgery · 20d

Cleared Apr 08, 1985

MISCELLANEOUS GENERAL SURGICAL CUSTOM KIT

K844597

General & Plastic Surgery · 133d

Cleared Oct 23, 1984

CATHETER INTRODUCER SYSTEM

K843641 · DYB

Cardiovascular · 36d

Cleared Oct 23, 1984

SUBCLAVIAN LEAD INTRODUCER SYS

K843642 · DYB

Cardiovascular · 36d

Xanmed Corp. - FDA 510(k) Cleared Devices

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