Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

PEREGRINE ILLUMINATING LASER PROBE MODEL PD600.10

K-Number: K031023 · 2003-06-27

ApplicantPeregrine Surgical , Ltd.
Decision Date2003-06-27
Product CodeHQF
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

PEREGRINE ILLUMINATING LASER PROBE MODEL PD600.10 is the device name listed in this FDA 510(k) record. The listed applicant is Peregrine Surgical , Ltd.. It received FDA 510(k) clearance on 2003-06-27 under 510(k) number K031023. The device is classified under product code HQF. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PEREGRINE ILLUMINATING LASER PROBE MODEL PD600.10?

PEREGRINE ILLUMINATING LASER PROBE MODEL PD600.10 is a medical device that received FDA 510(k) clearance on 2003-06-27. The listed applicant is Peregrine Surgical , Ltd.. The 510(k) number is K031023.

When did PEREGRINE ILLUMINATING LASER PROBE MODEL PD600.10 receive FDA 510(k) clearance?

PEREGRINE ILLUMINATING LASER PROBE MODEL PD600.10 received FDA 510(k) clearance on 2003-06-27, under 510(k) number K031023.

Who is the listed applicant for PEREGRINE ILLUMINATING LASER PROBE MODEL PD600.10?

The FDA 510(k) record lists Peregrine Surgical , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PEREGRINE ILLUMINATING LASER PROBE MODEL PD600.10?

The FDA product code for PEREGRINE ILLUMINATING LASER PROBE MODEL PD600.10 is HQF.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Peregrine Surgical , Ltd. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K132614PEREGRINE CURVED ILLUMINATING LASER PROBEK12299723GA CURVED ILLUMINATING LASER PROBEK122905PEREGRINE 23GA CURVED LASER PROBEK061024PEREGRINE SOFT TIP ASPIRATING LASER PROBE, MODEL PD720.60K024061PEREGRINE STRAIGHT LASER PROBE, MODEL PD6000.00K990518PEREGRINE WET SET, MODEL PD400.00

View all 18 devices →

Related Devices (Code: HQF)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K252979Voyager DSLT (430840610)Belkin Vision, Ltd.K251507INTEGRE LIOQuantel MedicalK251772Navilas Laser System 577sl (156691)Od-Os GmbHK243014EyeQ nanoECPEyeq, Inc.K240615Leos Laser and Endoscopy SystemBeaver-Visitec International, Inc.K242397LYNX PhotocoagulatorNorlase Aps

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑