510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K851033Substantially Equivalent

Syncortech Chlamydia Direct Speciman Kit

Syncor Intl. Corp., Sylmar CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K851033 is the FDA 510(k) clearance record for SYNCORTECH CHLAMYDIA DIRECT SPECIMAN KIT, a class I device, cleared for Syncor Intl. Corp. on under FDA product code LJP (Antiserum, Fluorescent, Chlamydia Trachomatis). FDA records list 31 510(k) clearances for Syncor Intl. Corp., from to . As of , FDA records show no recalls naming K851033.

Clearance record

Decision date
Received
(101 days to decision)
Product code
LJP Antiserum, Fluorescent, Chlamydia Trachomatis
Regulation
21 CFR 866.3120
Device class
Class I
Review panel
Microbiology
Applicant
Syncor Intl. Corp. 12847 Arroyo St., Sylmar 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