510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K993635Substantially Equivalent

Mdi Sm/rnp Test

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

K993635 is the FDA 510(k) clearance record for MDI SM/RNP TEST, a class II device, cleared for Micro Detect, Inc. on under FDA product code LJM (Antinuclear Antibody (Enzyme-Labeled), Antigen, Controls). FDA records list 11 510(k) clearances for Micro Detect, Inc., from to . As of , FDA records show no recalls naming K993635.

Clearance record

Decision date
Received
(75 days to decision)
Product code
LJM Antinuclear Antibody (Enzyme-Labeled), Antigen, Controls
Regulation
21 CFR 866.5100
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 LJM

Trailing 12 months

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

FDA records show no clearances under product code LJM in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code LJM, 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