Medical Device Manufacturer · US , Mobile , AL

Wuestec Medical, Inc. - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 1993

Recent clearances: PENSIL TRAUMA, MODEL WWS6100, XRT 600 R/F, WRF 0600, C-QUEST

View 9 510(k) Devices ↓

Total

Cleared

Denied

Wuestec Medical, Inc. has 9 FDA 510(k) cleared medical devices. Based in Mobile, US.

Historical record: 9 cleared submissions from 1993 to 1999. Primary specialty: Radiology.

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

Wuestec Medical, Inc. is one of 21484 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Wuestec Medical, Inc.

9 devices

1-9 of 9

Cleared Dec 21, 1999

PENSIL TRAUMA, MODEL WWS6100

K993962 · KPR

Radiology · 57d

Cleared Oct 25, 1999

XRT 600 R/F, WRF 0600

DX-480, ADD ON DIGITAL IMAGER

MOVABLE CANTILEVERED RADIOGRAPHIC TABLE XRT 100, 200 & 300

Wuestec Medical, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Wuestec Medical, Inc.

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