QL MULTIPULSE 2048— 510(k) K933299

Substantially Equivalent

Infimed, Inc.

FDA 510(k) clearance K933299 for QL MULTIPULSE 2048, Substantially Equivalent on 1993-11-03. Applicant: Infimed, Inc..

Clearance details

Applicant: Infimed, Inc.
Product code: Code JAA
Advisory panel: Radiology
Date received: 1993-07-07
Decision date: 1993-11-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Liverpool, NY, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code JAA

product code JAA

Other: 1
Total: 1

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.