ClearanceBrief
Company ยท US

Nordiclab Intl.

FDA 510(k) clearances and medical device recalls filed under this name, 1979 to 1980. Name variants (Inc, Corp, punctuation) are merged.

8510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
CDZRadioimmunoassay, Testosterones And Dihydrotestosterone1
CGIRadioimmunoassay, Estriol1
CHPRadioimmunoassay, Estradiol1
DBFFerritin, Antigen, Antiserum, Control1
JFHAcid Phosphatase (Prostatic), Tartrate Inhibited1
JLSRadioimmunoassay, Progesterone1
JMFRadioimmunoassay, Human Placental Lactogen1
JMGRadioimmunoassay (Two-Site Solid Phase), Ferritin1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Sep 26, 1980K801988NORDICLAB PROSTATIC ACID PHOSPHATASE RIA
Nordiclab Intl.
JFH
Sep 16, 1980K801989NORDICLAB FERRITIN IRMA TEST
Nordiclab Intl.
DBF
May 14, 1980K800922NORDICLAB PROGESTERONE RIA TEST
Nordiclab Intl.
JLS
May 14, 1980K800921NORDICLAB TESTOSTERONE RIA TEST
Nordiclab Intl.
CDZ
May 14, 1980K800920NORDICLAB ESTRADIOL RIA TEST
Nordiclab Intl.
CHP
Nov 13, 1979K792189NORDICLAB TOTAL ESTRIOL RIA TEST
Nordiclab Intl.
CGI
Jan 17, 1979K782157IRMA TEST, NORDICLAB FERRITIN
Nordiclab Intl.
JMG
Jan 10, 1979K782099RIA TEST, NORDICALB HPL
Nordiclab Intl.
JMF

Latest recalls

DateFirm and productCodeLinked 510(k)
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