Medical Device Manufacturer · US , San Diego , CA

Syntron Bioresearch, Inc. - FDA 510(k) Cleared Devices

26 submissions · 26 cleared · Since 1987

Recent clearances: QUICKSTRIP ONE STEP OPIATES TEST, QUICKPAC II ONE STEP OPIATES TEST, QUICKPAC II ONE STEP COCAINE TEST

26
Total
26
Cleared
0
Denied

Syntron Bioresearch, Inc. has 26 FDA 510(k) cleared medical devices. Based in San Diego, US.

Historical record: 26 cleared submissions from 1987 to 1999. Primary specialty: Chemistry.

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

510(k) submissions have been managed by California Department of Health Services as regulatory consultant.

FDA 510(k) Regulatory Record - Syntron Bioresearch, Inc.

26 devices
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