MDI RF TEST— 510(k) K993843

Substantially Equivalent

Micro Detect, Inc.

FDA 510(k) clearance K993843 for MDI RF TEST, Substantially Equivalent on 2000-01-11. Applicant: Micro Detect, Inc.. Device class: 2.

Clearance details

Applicant: Micro Detect, Inc.
Product code: Code DHR
Device class: Class 2
Regulation: 21 CFR 866.5775
Advisory panel: Immunology
Date received: 1999-11-12
Decision date: 2000-01-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Tustin, CA, US

Download summary PDF View on FDA.gov ↗

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More clearances from Micro Detect, Inc.

K003794 — ELISA TEST, SEROLOGY2001-03-30
K002358 — MDI GLIADIN A TEST2000-10-19
K002359 — MDI GLIADIN G TEST2000-10-19
K000934 — MDI SCL-70 TEST2000-04-07
K000477 — MDI DS-DNA TEST2000-03-01

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