ClearanceBrief
Company ยท US

Idt, A Division of Whittaker M.A. Bioproducts

FDA 510(k) clearances and medical device recalls filed under this name, 1977 to 1986. Name variants (Inc, Corp, punctuation) are merged.

5510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
DHNAntinuclear Antibody, Indirect Immunofluorescent, Antigen, Control2
DAKComplement C1q, Antigen, Antiserum, Control1
GQXAntiserum, Cf, Varicella-Zoster1
GREAntiserum, Fluorescent, Rubeola1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Feb 4, 1986K853540FIAX TEST KIT FOR VARICELLA ANTIBODY SEROLOGY
Idt, A Division of Whittaker M.A. Bioproducts
GQX
Oct 22, 1985K853067FIAX TEST KIT FOR MEASLES-G ANTIBODIES FLYORESCENT
Idt, A Division of Whittaker M.A. Bioproducts
GRE
Jan 3, 1979K782041FIAX TEST KIT
Idt, A Division of Whittaker M.A. Bioproducts
DHN
Jan 20, 1978K772219FIAX TEST FOR ANTI-RUBELLA ANTIBODY
Idt, A Division of Whittaker M.A. Bioproducts
DHN
Nov 30, 1977K772114FIAX C4 ASSAY
Idt, A Division of Whittaker M.A. Bioproducts
DAK

Latest recalls

DateFirm and productCodeLinked 510(k)
No recalls in this window.
Get alerts for these product codes