PEREGRINE 23GA CURVED LASER PROBE— 510(k) K122905

Substantially Equivalent

Peregrine Surgical , Ltd.

FDA 510(k) clearance K122905 for PEREGRINE 23GA CURVED LASER PROBE, Substantially Equivalent on 2013-04-30. Applicant: Peregrine Surgical , Ltd..

Clearance details

Applicant: Peregrine Surgical , Ltd.
Product code: Code HQB
Advisory panel: Ophthalmic
Date received: 2012-09-21
Decision date: 2013-04-30
Decision: Substantially Equivalent
Clearance type: Special
Location: New Britain, PA, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code HQB

product code HQB

Other: 2
Total: 2

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.