Medical Device Manufacturer · US , Anaheim , CA

Angiomed U.S., Inc. - FDA 510(k) Cleared Devices

24 submissions · 24 cleared · Since 1986

Total

Cleared

Denied

Angiomed U.S., Inc. has 24 FDA 510(k) cleared medical devices. Based in Anaheim, US.

Historical record: 24 cleared submissions from 1986 to 1988. Primary specialty: General & Plastic Surgery.

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

Angiomed U.S., 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 - Angiomed U.S., Inc.

24 devices

1-12 of 24

Cleared Jan 12, 1988

ANGIOMED INTRODUCING SETS

K874771 · DWB

Cardiovascular · 54d

Cleared Dec 02, 1987

ANGIOMED OSTY-CUT BONE BIOPSY NEEDLE

K874585 · DWO

General & Plastic Surgery · 23d

Cleared Jan 30, 1987

ANGIOMED URETERAL D&M SETS/URETEROSCOPY GUID STENT

K864225 · FAD

Gastroenterology & Urology · 94d

Cleared Oct 24, 1986

VESICO SUPRAPUBIC BLADDER DRAINAGE & EXCHANGE SETS

K863386 · KOB

Gastroenterology & Urology · 51d

Cleared Sep 29, 1986

ANGIOMED VAC-U-CUT BIOPSY NEEDLE

K862805 · GDM

General & Plastic Surgery · 69d

Cleared Sep 23, 1986

ANGIOMED HIGH PRESSURE CONNECTORS

K863446 · GCD

General & Plastic Surgery · 15d

Cleared Jul 17, 1986

ANGIOFLOW

K854910 · DQO

Cardiovascular · 220d

Cleared Apr 16, 1986

ANGIOMED GUIED WIRES

K854912 · DQX

Cardiovascular · 128d

Cleared Mar 14, 1986

UROFLEX

K854908 · FAD

Gastroenterology & Urology · 95d

Cleared Mar 11, 1986

ANGIOMED URETER DIATION SETS

K855076 · KOD

Gastroenterology & Urology · 82d

Cleared Mar 11, 1986

ANGIOMED PERCUTANEOUS TRANSHEPATIC CHOLANGIOGTAPHY

K855142 · FGE

Gastroenterology & Urology · 75d

Cleared Mar 11, 1986

ANGIOMED EXCHANGE DRAINAGE CATHETER SETS

K855143 · KOD

Gastroenterology & Urology · 75d

Angiomed U.S., Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Angiomed U.S., Inc.

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