FDA Device Intelligence
Home › INSIGHTEC LTD › Master Treatment Kit for 3.0T (GE) Type 1.0& 1.1 NonCE/FDA

Master Treatment Kit for 3.0T (GE) Type 1.0& 1.1 NonCE/FDA

INSIGHTEC LTD · Model SET001102 Master Treatment Kit for 3.0T (GE) Type 1.0& 1.1 NonCE/FDA · UDI-DI 07290015461887

POH Prescription
0
510(k) clearances
261
Adverse events (5 deaths)
0
Recalls
4
Facilities

Description

A Kit for 10 Neuro treatment (Master Treatment Kit for 3.0T (GE) Type 1.0& 1.1 NonCE/FDA). Kit content: Part Description SET001045 EXABLATE NEURO PATIENT TREATMENT KIT 3.0T GE (5) X 2 units

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.