Home / 510(k) Clearances / K790250

510(k) K790250

LIQUISOL CORTISOL RIA TEST KIT by Damon Corp.

K790250 is an FDA 510(k) premarket notification submitted by Damon Corp. for the device "LIQUISOL CORTISOL RIA TEST KIT". The FDA issued a decision of Substantially Equivalent on April 4, 1979. Damon Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 4, 1979
Date Received
February 6, 1979
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Other clearances by Damon Corp.

  • K874865 — DAMON D.E.T.E.C.T IMAGE ENHANCER (December 23, 1987)
  • K831826 — ADRENOCORTICOTROPIN RADIO-IMMUNOASSAY (July 18, 1983)
  • K820686 — LIQUISOL PROGESTERONE RADIOIMMUNO (April 1, 1982)
  • K802661 — LIQUISOL TESTOSTERONE RADIOIMM. TEST KIT (December 10, 1980)
  • K782124 — IEC CENTRA-7 CENTRIFUGE MODEL 2362 (February 26, 1979)
  • K781012 — RIA TEST KIT SYS. DAMON KIQUISOL FREE (July 27, 1978)
  • K780207 — LIQUISOL DIGOXIN RIA TEST KIT (February 23, 1978)
  • K770918 — LIQUI SOL T4 RIA TEST KIT (June 17, 1977)
  • K770606 — ANALYZEO, PLASMA, BLOOD, COLYSAGRAPH (May 6, 1977)
  • K761013 — SPINETTE CENTRIFUGE (November 16, 1976)

FDA data resources