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FDA 510(k)

PEREGRINE CURVED ILLUMINATING LASER PROBE

K-Number: K132614 · 2013-11-14

ApplicantPeregrine Surgical , Ltd.
Decision Date2013-11-14
Product CodeHQB
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

PEREGRINE CURVED ILLUMINATING LASER PROBE 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 2013-11-14 under 510(k) number K132614. The device is classified under product code HQB. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PEREGRINE CURVED ILLUMINATING LASER PROBE?

PEREGRINE CURVED ILLUMINATING LASER PROBE is a medical device that received FDA 510(k) clearance on 2013-11-14. The listed applicant is Peregrine Surgical , Ltd.. The 510(k) number is K132614.

When did PEREGRINE CURVED ILLUMINATING LASER PROBE receive FDA 510(k) clearance?

PEREGRINE CURVED ILLUMINATING LASER PROBE received FDA 510(k) clearance on 2013-11-14, under 510(k) number K132614.

Who is the listed applicant for PEREGRINE CURVED ILLUMINATING LASER PROBE?

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 CURVED ILLUMINATING LASER PROBE?

The FDA product code for PEREGRINE CURVED ILLUMINATING LASER PROBE is HQB.

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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.

K12299723GA CURVED ILLUMINATING LASER PROBEK122905PEREGRINE 23GA CURVED LASER PROBEK061024PEREGRINE SOFT TIP ASPIRATING LASER PROBE, MODEL PD720.60K031023PEREGRINE ILLUMINATING LASER PROBE MODEL PD600.10K024061PEREGRINE STRAIGHT LASER PROBE, MODEL PD6000.00K990518PEREGRINE WET SET, MODEL PD400.00

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Related Devices (Code: HQB)

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.

K220263Vortex Surgical Laser Probes, Vortex Surgical Illuminated Laser Probes, Vortex Surgical Endoilluminators, Vortex Surgical ChandeliersVortex Surgical, Inc.K191846MAXReach Laser ProbeVortex Surgical, Inc.K182646Vitreq disposable laser probes, light fibers and ChandelierVitreQ BVK12299723GA CURVED ILLUMINATING LASER PROBEPeregrine Surgical , Ltd.K122905PEREGRINE 23GA CURVED LASER PROBEPeregrine Surgical , Ltd.K113857SYNERGETICS DIRECTIONAL ENDOOCULAR LASER PROBESynergetics, Inc.

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.

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