Medical Device Manufacturer · US , Mchenry , IL

Syntex Corp. - FDA 510(k) Cleared Devices

10 submissions · 10 cleared · Since 1976

Total

Cleared

Denied

Syntex Corp. has 10 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 10 cleared submissions from 1976 to 1992. Primary specialty: Radiology.

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

FDA 510(k) Regulatory Record - Syntex Corp.

10 devices

1-10 of 10

Cleared Apr 17, 1992

TXIT D.A.U. BARBITURATE ASSAY (MODIFICATION)

K920314 · DIS

Toxicology · 85d

Cleared Oct 24, 1984

SURGIPRESS SURGICAL LOOP

K843593 · HRQ

General & Plastic Surgery · 42d

FIBER OPTIC HANDPIECE

K780483 · EFB

Dental · 32d

Cleared Jan 03, 1977

OPUS I OPTION - FIBER OPTIC L SYSTEM

HI-SENSITIVITY MODE OPTION FOR S60-1A

K761332 · JAK

Radiology · 3d

Cleared Dec 23, 1976

OPTIONS FOR STAR DENTAL OPUS I

K761264 · DYN

Dental · 7d

Cleared Nov 24, 1976

COMPUTERIZED TOMOGRAPHY SCANNER

K761033 · JAK

Radiology · 9d

Syntex Corp. - FDA 510(k) Cleared Devices

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