510(k) Report

510(k) · Cleared

Cleared

Jamieson JT-CRP Cine Film Processor

K913241510(k) TraditionalCleared Sep 24, 199164-day reviewClass II21 CFR 892.1900

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Jamieson Film Co. · IXX Processor, Cine Film

Cleared on Sep 24, 1991 after a 64-day review. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known. 1 later device descends from it.

Decided
Sep 24, 1991
Review
64 days
Class
Class II
Product code
IXX
Recalls
None
Predicates
0

1 later device descends from it, 1 citing it directly.

Descendants, by year cleared 1996: 1 descendant cleared1990200020102020
  1. This deviceK913241 Jamieson JT-CRP Cine Film ProcessorJamieson Film Co. · 1991
  2. Descendant · cites it directly · 0 of its ownK963334 Jamieson Model 2100 Cine Film Processor and Kodak Cineflure…Jamieson Film Co. · 1996

Most influential descendants

Showing 1 of 1 · See all
  • K963334Jamieson Model 2100 Cine Film Processor and Kodak Cineflure Processor Model 2100Jamieson Film Co. · 1996 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K913241Jamieson JT-CRP Cine Film ProcessorJamieson Film Co.1991—
+1K963334Jamieson Model 2100 Cine Film Processor and Kodak Cineflure Processor Model 2100Jamieson Film Co.1996—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
199610
FIG. 1 — Lineage of K913241, 1991–1996Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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Notable FDA decisions, review times and new Class I recalls. See an issue.

Sources: FDA 510(k) database (decision fields), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

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What was it cleared against?

FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

What descends from it? (1)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K963334Jamieson Model 2100 Cine Film Processor and Kodak Cineflure Processor Model 2100Jamieson Film Co.19960

Has anything in its family been recalled? (0 Class I)

No FDA recall names this device.

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • Of its descendants, K963334 (Jamieson Film Co., 1996) has gone furthest, with 0 descendants of its own.

How does its category compare?

All IXX devices

IXX Processor, Cine Film: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · IXX

FDA has decided no IXX device since 2007.

Median 510(k) review, days · IXX

Too few IXX 510(k)s in any year since 2007 to give a median.

Recalls per year · IXX

No recall names IXX since 2007.

Adverse event reports per year · IXX

No MAUDE report names IXX since 2007.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20070—00
20080—00
20090—00
20100—00
20110—00
20120—00
20130—00
20140—00
20150—00
20160—00
20170—00
20180—00
20190—00
20200—00
20210—00
20220—00
20230—00
20240—00
20250—00
20260—0—
Cite this page

510(k) Report. “K913241: Jamieson JT-CRP Cine Film Processor.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K913241

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Record history
  • FDA decision record loaded May 2, 2026
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026