Medical Device Manufacturer · US , Hyattsville , MD

Dhason Brothers, Inc. - FDA 510(k) Cleared Devices

14 submissions · 14 cleared · Since 1989

Total

Cleared

Denied

Dhason Brothers, Inc. has 14 FDA 510(k) cleared orthopedic devices. Based in Hyattsville, US.

Historical record: 14 cleared submissions from 1989 to 1989.

Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Dhason Brothers, Inc.

14 devices

1-14 of 14

Cleared Feb 13, 1989

IMPACTOR FOR FEMORAL HEAD

GOUGES FOR FEMORAL HEADS

K890160 · LXH

Orthopedic · 35d

Cleared Feb 13, 1989

THOMPSON TYPE RASP W/TOMMY BAR

K890161 · LXH

Orthopedic · 35d

Cleared Feb 13, 1989

EXTRACTOR FOR AUSTIN MOORE FEMORAL HEAD

K890162 · LXH

Orthopedic · 35d

Cleared Feb 13, 1989

AUSTIN MOORE HALLOW CHISEL

RETRACTOR, SELF-RETAINING

General & Plastic Surgery · 25d

General & Plastic Surgery · 25d

Dhason Brothers, Inc. - FDA 510(k) Cleared Devices

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