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510(k) K844767

RADIOIMMUNOASSAY OF HUMAN SERUM PLASMA OR URINE TO by Biotecx Laboratories, Inc. — Product Code CGI

K844767 is an FDA 510(k) premarket notification submitted by Biotecx Laboratories, Inc. for the device "RADIOIMMUNOASSAY OF HUMAN SERUM PLASMA OR URINE TO". The FDA issued a decision of Substantially Equivalent on February 1, 1985. The device falls under product code CGI (Radioimmunoassay, Estriol), a Class I device regulated under 21 CFR 862.1265. Biotecx Laboratories, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 1, 1985
Date Received
December 7, 1984
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Radioimmunoassay, Estriol
Device Class
Class I
Regulation Number
862.1265
Review Panel
CH
Submission Type

Other clearances by Biotecx Laboratories, Inc.

  • K982298 — OPTICOAT T4 EIA KIT (February 3, 1999)
  • K981824 — OPTICOAT T3 EIA KIT (December 22, 1998)
  • K895407 — CORTISOL CLASP-BEAD EIA KIT (October 19, 1989)
  • K893620 — T3 CLASP-BEAD EIA KIT (August 11, 1989)
  • K892853 — T4 CLASP-BEAD EIA KIT (May 22, 1989)
  • K883765 — TBG 125I RIA KIT, RADIOIMMUNO. OF SERUM THYROXINE (October 31, 1988)
  • K871211 — PROGESTERONE CLASP RADIOIMMUNOASSAY KIT (April 13, 1987)
  • K863188 — HPL RIA KIT (September 25, 1986)
  • K854876 — ALDOSTERONE DIRECT RIA KIT (March 17, 1986)
  • K851540 — ESTRADIOL DIRECT RIA KIT (June 6, 1985)

Other clearances for product code CGI

  • K974721 — UNCONJUGATED ESTRIOL ASSAY FOR THE BAYER IMMUNO 1 SYSTEM (IN VITRO DIAGNOSTIC SY (March 3, 1998)
  • K962875 — ACTIVE ULTRASENSITIVE UNCONJUGATED ESTRIOL EIA (August 23, 1996)
  • K955356 — ACTIVE ULTRA-SENSITIVE UNCONJUGATED ESTRIOL (May 15, 1996)
  • K932989 — COAT-A-COUNT FREE ESTRIOL (December 19, 1994)
  • K944490 — AUTODELFIA UNCONJUGATED ESTRIOL (UE3) KIT (December 9, 1994)
  • K920576 — AMERLEX-M HIGH SENSITIVITY UNCONJUGATED ESTRIOL (March 23, 1992)
  • K903359 — MICROZYME UNCONJUGATED ESTRIOL ENZYME IMMUNO KIT (August 22, 1990)
  • K860900 — IMMPULSE FREE ESTRIOL ASSAY REAGENTS (April 28, 1986)
  • K850787 — SOLID PHASE FREE ESTRIOL ENZYME IMMUNOASSAY (March 26, 1985)
  • K844511 — TDX TOTAL ESTRIOL (January 18, 1985)

FDA data resources