MMS T3 UPTAKE— 510(k) K861262

Substantially Equivalent

Micromedic Systems

FDA 510(k) clearance K861262 for MMS T3 UPTAKE, Substantially Equivalent on 1986-05-23. Applicant: Micromedic Systems. Device class: 2.

Clearance details

Applicant: Micromedic Systems
Product code: Code KHQ
Device class: Class 2
Regulation: 21 CFR 862.1715
Advisory panel: Clinical Chemistry
Date received: 1986-04-04
Decision date: 1986-05-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Horsham, PA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KHQ

K981375 — ACE T UPTAKE REAGENT TU CALIBRATORS1998-06-10
K980088 — T-UPTAKE MICROPLATE EIA1998-02-04
K970539 — CHIRON DIAGNOSTICS ACS:180TU P1997-03-24
K964308 — VITROS IMMUNODIAGNOSTICS PRODUCTS T3 UPTAKE REAGENT PACK (GEM.1025) AND T3 UPTAKE CALIBRATORS (GEM.C025)1996-11-27
K961488 — ELECSYS T-UPTAKE ASSAY1996-06-12

More clearances from Micromedic Systems

K923643 — MEDICOOL1993-03-31
K872309 — MICROMEDIC COMBOSTAT LH/FSH KIT1987-07-31
K870904 — MICROMEDIC NEONATAL TSH MONOCLONAL IRMA KIT1987-05-26
K871008 — MICROMEDIC NEONATAL T4 KIT1987-05-26
K871505 — AUTOPAK NEONATAL TSH MONOCLONAL IRMA KIT1987-05-26

Data sourced from openFDA. This site is unofficial and independent of the FDA.