K-number	K113380
Device name	PROSTIVA RF THERAPY HAND PIECE PROSTIVA RF THERAPY RF GENERATOR
Applicant	Medtronic, Inc.
Product code	GEI
Device class	Class II
Decision date	Nov 15, 2012
Decision	Substantially Equivalent
Regulation	—

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 →

PROSTIVA RF THERAPY HAND PIECE PROSTIVA RF THERAPY RF GENERATOR

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