510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K850629Substantially Equivalent

Innofluor Theophylline

Innotron Diagnostics, Irvine CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K850629 is the FDA 510(k) clearance record for INNOFLUOR THEOPHYLLINE, a class II device, cleared for Innotron Diagnostics on under FDA product code LGS (Fluorescence Polarization Immunoassay, Theophylline). FDA records list 6 510(k) clearances for Innotron Diagnostics, from to . As of , FDA records show no recalls naming K850629.

Clearance record

Decision date
Received
(21 days to decision)
Product code
LGS Fluorescence Polarization Immunoassay, Theophylline
Regulation
21 CFR 862.3880
Device class
Class II
Review panel
Clinical Toxicology
Applicant
Innotron Diagnostics 6-A Faraday, Irvine CA
Third party review
No

Clearances, product code LGS

Trailing 12 months

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

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