510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K993843Substantially Equivalent

Mdi RF Test

Micro Detect, Inc., Tustin CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K993843 is the FDA 510(k) clearance record for MDI RF TEST, a class II device, cleared for Micro Detect, Inc. on under FDA product code DHR (System, Test, Rheumatoid Factor). FDA records list 11 510(k) clearances for Micro Detect, Inc., from to . As of , FDA records show no recalls naming K993843.

Clearance record

Decision date
Received
(60 days to decision)
Product code
DHR System, Test, Rheumatoid Factor
Regulation
21 CFR 866.5775
Device class
Class II
Review panel
Immunology
Applicant
Micro Detect, Inc. 2852 Walnut Ave., Suite H-1, Tustin CA
510(k) summary
Summary
Third party review
No

Clearances, product code DHR

Trailing 12 months

FDA records hold no clearances under product code DHR in the trailing twelve months.

FDA records show no clearances under product code DHR in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code DHR, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260