PEREGRINE ILLUMINATING LASER PROBE MODEL PD600.10— 510(k) K031023

Substantially Equivalent

Peregrine Surgical , Ltd.

FDA 510(k) clearance K031023 for PEREGRINE ILLUMINATING LASER PROBE MODEL PD600.10, Substantially Equivalent on 2003-06-27. Applicant: Peregrine Surgical , Ltd..

Clearance details

Applicant: Peregrine Surgical , Ltd.
Product code: Code HQF
Advisory panel: Ophthalmic
Date received: 2003-03-31
Decision date: 2003-06-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: New Britain, PA, US

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Adverse events under product code HQF

product code HQF

Injury: 166
Other: 1
Total: 167

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.