ClearanceBrief
Company ยท US

Syntex Corp.

FDA 510(k) clearances and medical device recalls filed under this name, 1976 to 1992. Name variants (Inc, Corp, punctuation) are merged.

10510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
JAKSystem, X-Ray, Tomography, Computed4
DISEnzyme Immunoassay, Barbiturate1
DYNMouthpiece, Saliva Ejector1
EAYLight, Fiber Optic, Dental1
EFBHandpiece, Air-Powered, Dental1
EJJAlloy, Amalgam1
HRQHemostat1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Apr 17, 1992K920314TXIT D.A.U. BARBITURATE ASSAY (MODIFICATION)
Syntex Corp.
DIS
Oct 24, 1984K843593SURGIPRESS SURGICAL LOOP
Syntex Corp.
HRQ
Jul 27, 1978K780997AMALGAM ALLOY
Syntex Corp.
EJJ
Jun 2, 1978K780769S-100 CT SCANNER
Syntex Corp.
JAK
Apr 28, 1978K780483FIBER OPTIC HANDPIECE
Syntex Corp.
EFB
Jan 3, 1977K761331OPUS I OPTION - FIBER OPTIC L SYSTEM
Syntex Corp.
EAY
Dec 30, 1976K761332HI-SENSITIVITY MODE OPTION FOR S60-1A
Syntex Corp.
JAK
Dec 30, 1976K761330SYNTEX SYSTEM 6000
Syntex Corp.
JAK
Dec 23, 1976K761264OPTIONS FOR STAR DENTAL OPUS I
Syntex Corp.
DYN
Nov 24, 1976K761033COMPUTERIZED TOMOGRAPHY SCANNER
Syntex Corp.
JAK

Latest recalls

DateFirm and productCodeLinked 510(k)
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