JETPACK 2.0— 510(k) K111024

Substantially Equivalent

Philips Medical Systems (Cleveland), Inc.

FDA 510(k) clearance K111024 for JETPACK 2.0, Substantially Equivalent on 2011-04-21. Applicant: Philips Medical Systems (Cleveland), Inc..

Clearance details

Applicant: Philips Medical Systems (Cleveland), Inc.
Product code: Code LLZ
Advisory panel: Radiology
Date received: 2011-04-12
Decision date: 2011-04-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Jose, CA, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code LLZ

product code LLZ

Death: 13
Total: 13

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.