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510(k) K863849

LIQUI-SERA COMBO LIGAND/TDM CONTROLS by Biodiagnostic Intl — Product Code JJY

K863849 is an FDA 510(k) premarket notification submitted by Biodiagnostic Intl for the device "LIQUI-SERA COMBO LIGAND/TDM CONTROLS". The FDA issued a decision of Substantially Equivalent on November 24, 1986. The device falls under product code JJY (Multi-Analyte Controls, All Kinds (Assayed)), a Class I device regulated under 21 CFR 862.1660. Biodiagnostic Intl has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 24, 1986
Date Received
September 30, 1986
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Multi-Analyte Controls, All Kinds (Assayed)
Device Class
Class I
Regulation Number
862.1660
Review Panel
CH
Submission Type

Other clearances by Biodiagnostic Intl

  • K031296 — LIQUI-HEME GLYCO A1C ASSAY (October 15, 2004)
  • K881430 — LIQUI-SERA SERUM ALCOHOL CONTROLS (July 8, 1988)
  • K874459 — LIQUI-SERA SPINAL FLUID CONTROL (December 29, 1987)
  • K853906 — LIQUI-SERA CHEMISTRY CONTROLS (COMPREHENSIVE) (October 4, 1985)
  • K853887 — LIQUI-SERA CHEM. MULTIPLE CALIBRATORS (September 30, 1985)
  • K842668 — LIQUI-HEME HEMOGLOBIN CALIBRATORS (March 5, 1985)
  • K840618 — LIQUI-URA CHEMISTRY URINE CONTROLS (April 4, 1984)
  • K834398 — LIQUI-SERA TDM CALIBRATORS (February 3, 1984)
  • K834259 — LIQUI-URA TOXIC URINE CONTROL (January 30, 1984)
  • K831278 — LIQUI-SERA ANTICONVULSANTS CONTROLS (May 27, 1983)

Other clearances for product code JJY

  • K162530 — Multichem IA Plus (March 31, 2017)
  • K163629 — Audit MicroControls Linearity FD Tumor Markers II (March 10, 2017)
  • K163015 — Liquichek Tumor Marker Control-Level 1; Liquichek Tumor Marker Control-Level 2; (January 10, 2017)
  • K153712 — VK-3 Verification Kit, VK-4 Verification Kit, VK-R5 Verification Kit, VK-R7 Veri (January 28, 2016)
  • K150300 — Liquichek Cardiac Markers Plus Control LT (December 11, 2015)
  • K142964 — VALIDATE Anemia Calibration Verification/ Linearity Test Kit (April 30, 2015)
  • K143379 — Liquichek Maternal Serum II Control (March 13, 2015)
  • K143573 — Audit MicroControls Linearity FD Tumor Markers II (January 16, 2015)
  • K140971 — LIQUID ASSAYED CHEMISTRY CONTROL PREMIUM PLUS LEVEL 1,2 AND LEVEL 3. (December 8, 2014)
  • K142978 — Audit MicroControls Linearity LQ Special Diabetes (November 20, 2014)

FDA data resources