K-number	K012010
Device name	MODIFICATION TO LR 5200 FILM RECORDER
Applicant	Agfa Corp.
Product code	LMC
Device class	Class II
Decision date	Sep 20, 2001
Decision	Substantially Equivalent
Regulation	892.2040

AI Summary

AI extraction for this record is queued and will appear within 24 hours. View full FDA record →

Source

View the full FDA submission: accessdata.fda.gov

Researching this as a predicate?

Want a transparent AI-ranking score, AI-discovered related predicates, ongoing safety and warning-letter monitoring, full predicate chain lineage, and a drafted SE rationale — all saved to your own project? That's what an account adds.

Start free trial →

Building an AI or ML-enabled device? Predicate search, PCCP tracking, and AI-specific FDA intelligence — built exclusively for AI/ML devices. Try AIFDA Intel →

MODIFICATION TO LR 5200 FILM RECORDER

Everything you need for a 510(k) submission. Nothing you don't.