Medical Device Manufacturer · US , San Diego , CA

Sequal Technologies, Inc. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2001
4
Total
4
Cleared
0
Denied

Sequal Technologies, Inc. has 4 FDA 510(k) cleared medical devices. Based in San Diego, US.

Historical record: 4 cleared submissions from 2001 to 2009. Primary specialty: Anesthesiology.

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

FDA 510(k) Regulatory Record - Sequal Technologies, Inc.
4 devices
1-4 of 4
Cleared Oct 20, 2009
OMNI 2 OXYGEN SYSTEM
K083163 · CAW
Anesthesiology · 358d
Cleared Sep 10, 2004
INTEGRA OXYGEN CONCENTRATOR, MODEL 6323A-OM-10
K042262 · CAW
Anesthesiology · 18d
Cleared Mar 27, 2002
OMNI OXYGEN SYSTEM, MODEL 1000
K013931 · CAW
Anesthesiology · 119d
Cleared Jun 04, 2001
INTEGRA OXYGEN CONCENTRATORS MODEL 6400-OM
K003472 · CAW
Anesthesiology · 208d
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