PEREGRINE ILLUMINATING LASER PROBE MODEL PD600.10— 510(k) K031023
Substantially EquivalentPeregrine 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.. Device class: 2.
Clearance details
- Applicant
- Peregrine Surgical , Ltd.
- Product code
- Code HQF
- Device class
- Class 2
- Regulation
- 21 CFR 886.4390
- Advisory panel
- Ophthalmic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- New Britain, PA, US
Recent devices under product code HQF
view allMore clearances from Peregrine Surgical , Ltd.
view allAdverse events under product code HQF
product code HQF- Injury
- 166
- Other
- 1
- Total
- 167
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Recalls naming K031023
K-number listed on FDA's recall recordMatched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K031023.
Data sourced from openFDA. This site is unofficial and independent of the FDA.