Medical Device Manufacturer · US , Paso Robles , CA

Allied Biomedical Corp. - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 1995

Total

Cleared

Denied

Allied Biomedical Corp. has 9 FDA 510(k) cleared medical devices. Based in Paso Robles, US.

Historical record: 9 cleared submissions from 1995 to 1998. Primary specialty: General & Plastic Surgery.

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

Allied Biomedical Corp. 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 - Allied Biomedical Corp.

9 devices

1-9 of 9

Cleared Aug 05, 1998

KELOCATE SHEETING

K982051 · MDA

General & Plastic Surgery · 55d

Cleared Jul 18, 1997

DURALASTIC ANATOMICAL CHIN IMPLANTS

K971478 · FWP

General & Plastic Surgery · 86d

Cleared Jul 18, 1997

DURALASTIC ANATOMICAL MALAR IMPLANTS

K971479 · LZK

General & Plastic Surgery · 86d

Cleared Jul 18, 1997

DURALASTIC ANATOMICAL NASAL IMPLANTS

K971481 · FZE

General & Plastic Surgery · 86d

Cleared May 28, 1997

DURALASTIC I AND DURALASTIC II

K971480 · MIB

General & Plastic Surgery · 35d

Cleared Feb 08, 1996

DURALASTIC I

K955368 · MIB

General & Plastic Surgery · 78d

Cleared Feb 08, 1996

DURALASTIC II

K955370 · MIB

General & Plastic Surgery · 78d

Cleared Jan 26, 1996

DURALASTIC SILICONE TUBING

K955433 · KGZ

General & Plastic Surgery · 59d

Cleared Nov 29, 1995

KELOCOTE

K954413 · MDA

General & Plastic Surgery · 69d

Allied Biomedical Corp. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Allied Biomedical Corp.

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