510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K915332Substantially Equivalent

Model 795 Fluorometer/densitometer

Ciba Corning Diagnostics Corp., East Walpole MA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K915332 is the FDA 510(k) clearance record for MODEL 795 FLUOROMETER/DENSITOMETER, a class I device, cleared for Ciba Corning Diagnostics Corp. on under FDA product code JQT (Densitometer/Scanner (Integrating, Reflectance, Tlc, Radiochromat.) Clinica). FDA records list 125 510(k) clearances for Ciba Corning Diagnostics Corp., from to . As of , FDA records show no recalls naming K915332.

Clearance record

Decision date
Received
(84 days to decision)
Product code
JQT Densitometer/Scanner (Integrating, Reflectance, Tlc, Radiochromat.) Clinica
Regulation
21 CFR 862.2400
Device class
Class I
Review panel
Clinical Chemistry
Applicant
Ciba Corning Diagnostics Corp. 333 Coney St., East Walpole MA
510(k) summary
Statement
Third party review
No

Clearances, product code JQT

Trailing 12 months

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

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