PEGASYS ULTRA— 510(k) K993946

Substantially Equivalent

Adac Laboratories

FDA 510(k) clearance K993946 for PEGASYS ULTRA, Substantially Equivalent on 2000-03-09. Applicant: Adac Laboratories.

Clearance details

Applicant: Adac Laboratories
Product code: Code LLZ
Advisory panel: Radiology
Date received: 1999-11-19
Decision date: 2000-03-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Milpitas, 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.