510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K963334Substantially Equivalent

Jamieson Model 2100 Cine Film Processor and Kodak Cineflure Processor Model 2100

Jamieson Film Co., Dallas TX / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K963334 is the FDA 510(k) clearance record for JAMIESON MODEL 2100 CINE FILM PROCESSOR AND KODAK CINEFLURE PROCESSOR MODEL 2100, a class II device, cleared for Jamieson Film Co. on under FDA product code IXX (Processor, Cine Film). FDA records list 6 510(k) clearances for Jamieson Film Co., from to . As of , FDA records show no recalls naming K963334.

Clearance record

Decision date
Received
(16 days to decision)
Product code
IXX Processor, Cine Film
Regulation
21 CFR 892.1900
Device class
Class II
Review panel
Radiology
Applicant
Jamieson Film Co. 10425 Olympic Dr., Dallas TX
510(k) summary
Summary
Third party review
No

Clearances, product code IXX

Trailing 12 months

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

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