Home / 510(k) Clearances / K162530

510(k) K162530

Multichem IA Plus by Techno-Path Manufacturing — Product Code JJY

K162530 is an FDA 510(k) premarket notification submitted by Techno-Path Manufacturing for the device "Multichem IA Plus". The FDA issued a decision of Substantially Equivalent on March 31, 2017. The device falls under product code JJY (Multi-Analyte Controls, All Kinds (Assayed)), a Class I device regulated under 21 CFR 862.1660. Techno-Path Manufacturing has at least 6 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 31, 2017
Date Received
September 9, 2016
Clearance Type
Abbreviated
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 Techno-Path Manufacturing

  • K242492 — Multichem ID-G (09339892190); Multichem ID-G (SR102G); Multichem ID-G (SR102MG); (December 30, 2025)
  • K132751 — MULTICHEM S PLUS / S PLUS (ASSAYED) (October 22, 2013)
  • K131993 — MULTICHEM U (October 15, 2013)
  • K131992 — MULTICHEM P (September 25, 2013)
  • K132174 — MULTICHEM WBT (September 20, 2013)
  • K132091 — MULTICHEM IA AND IA PLUS (September 20, 2013)

Other clearances for product code JJY

  • 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)
  • K133676 — ABX PENTRA MICRO ALB CONTROL L/H (July 11, 2014)

FDA data resources