510(K) CLEARANCES 51 ▲2RECALLS POSTED 25 ▲2CLASS I 1PMA DECISIONS 50 ▲13WEEK ENDING / FDA DATA AS OF
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K963613Substantially Equivalent

Immulite Rubella Igg

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

K963613 is the FDA 510(k) clearance record for IMMULITE RUBELLA IGG, a class II device, cleared for Diagnostic Products Corp. on under FDA product code LFX (Enzyme Linked Immunoabsorbent Assay, Rubella). FDA records list 1,204 510(k) clearances for Siemens Healthcare Diagnostics Inc., from to . As of , FDA records show no recalls naming K963613.

Clearance record

Decision date
Received
(204 days to decision)
Product code
LFX Enzyme Linked Immunoabsorbent Assay, Rubella
Regulation
21 CFR 866.3510
Device class
Class II
Review panel
Microbiology
Applicant
Diagnostic Products Corp. 5700 W. 96th St., Los Angeles CA
510(k) summary
Summary
Third party review
No

Clearances, product code LFX

Trailing 12 months

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

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