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FDA 510(k)

PEREGRINE TAPERED DIFFUSION PROBE

K-Number: K980025 · 1998-03-31

ApplicantPeregrine Surgical , Ltd.
Decision Date1998-03-31
Product CodeMPA
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

PEREGRINE TAPERED DIFFUSION 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 1998-03-31 under 510(k) number K980025. The device is classified under product code MPA. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PEREGRINE TAPERED DIFFUSION PROBE?

PEREGRINE TAPERED DIFFUSION PROBE is a medical device that received FDA 510(k) clearance on 1998-03-31. The listed applicant is Peregrine Surgical , Ltd.. The 510(k) number is K980025.

When did PEREGRINE TAPERED DIFFUSION PROBE receive FDA 510(k) clearance?

PEREGRINE TAPERED DIFFUSION PROBE received FDA 510(k) clearance on 1998-03-31, under 510(k) number K980025.

Who is the listed applicant for PEREGRINE TAPERED DIFFUSION 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 TAPERED DIFFUSION PROBE?

The FDA product code for PEREGRINE TAPERED DIFFUSION PROBE is MPA.

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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.

K132614PEREGRINE CURVED ILLUMINATING LASER PROBEK12299723GA 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 PD6000.00

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Related Devices (Code: MPA)

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.

K253468Nova Eye iTrack™ 250A Canaloplasty Microcatheter (iTrack™ 250A)Nova Eye, Inc.K242184Alcon 27GA Chandelier (8065000252); Alcon 27+ DS Wide Angle Endoilluminator (8065000253); Alcon 27+ DS Endoilluminator (8065000256);Alcon Laboratories, Inc.K233653Midfield Light Pipe, 23ga (3269.M06-00); Midfield Light Pipe, 25ga (3269.M05-00); Midfield Light Pipe, 27ga (3269.M04-00)Peregrine Surgical, LLCK221872ITrack Advance Canaloplasty Microcatheter with Advanced Delivery SystemNova Eye Inc. (Business Name Nova Eye Medical)K202670Nam illumination probe with chopperOculight , Ltd.K080067ISCIENCE INTERVENTIONAL OPHTHALMIC MICROCATHETERIscience Interventional

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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