QUIKPAGE SCANNER— 510(k) K822582

Substantially Equivalent

Agilent Technologies

FDA 510(k) clearance K822582 for QUIKPAGE SCANNER, Substantially Equivalent on 1982-09-21. Applicant: Agilent Technologies.

Clearance details

Applicant: Agilent Technologies
Product code: Code DPS
Advisory panel: Cardiovascular
Date received: 1982-08-25
Decision date: 1982-09-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code DPS

product code DPS

Death: 7
Total: 7

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.