510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K900870Substantially Equivalent

Pathodx Chlamydia Trachomatis Direct Specimen Test

Siemens Healthcare Diagnostics Inc., Los Angeles CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K900870 is the FDA 510(k) clearance record for PATHODX CHLAMYDIA TRACHOMATIS DIRECT SPECIMEN TEST, a class I device, cleared for Diagnostic Products Corp. on under FDA product code LJP (Antiserum, Fluorescent, Chlamydia Trachomatis). FDA records list 1,204 510(k) clearances for Siemens Healthcare Diagnostics Inc., from to . As of , FDA records show no recalls naming K900870.

Clearance record

Decision date
Received
(51 days to decision)
Product code
LJP Antiserum, Fluorescent, Chlamydia Trachomatis
Regulation
21 CFR 866.3120
Device class
Class I
Review panel
Microbiology
Applicant
Diagnostic Products Corp. 5700 W. 96th St., Los Angeles CA
Third party review
No

Clearances, product code LJP

Trailing 12 months

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

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