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FDA 510(k)

PEREGRINE OPTIPORT VITRECTOMY PROBE MODEL PD500.20

K-Number: K980399 · 1998-04-30

ApplicantPeregrine Surgical , Ltd.
Decision Date1998-04-30
Product CodeHQE
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

PEREGRINE OPTIPORT VITRECTOMY PROBE MODEL PD500.20 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 1998-04-30 under 510(k) number K980399. The device is classified under product code HQE. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PEREGRINE OPTIPORT VITRECTOMY PROBE MODEL PD500.20?

PEREGRINE OPTIPORT VITRECTOMY PROBE MODEL PD500.20 is a medical device that received FDA 510(k) clearance on 1998-04-30. The listed applicant is Peregrine Surgical , Ltd.. The 510(k) number is K980399.

When did PEREGRINE OPTIPORT VITRECTOMY PROBE MODEL PD500.20 receive FDA 510(k) clearance?

PEREGRINE OPTIPORT VITRECTOMY PROBE MODEL PD500.20 received FDA 510(k) clearance on 1998-04-30, under 510(k) number K980399.

Who is the listed applicant for PEREGRINE OPTIPORT VITRECTOMY PROBE MODEL PD500.20?

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 OPTIPORT VITRECTOMY PROBE MODEL PD500.20?

The FDA product code for PEREGRINE OPTIPORT VITRECTOMY PROBE MODEL PD500.20 is HQE.

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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: HQE)

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.

K212763UniVit HE, UniVit UHSVisioncare Devices, LLCK170183Cetus system, Cetus probeA.R.C Laser GmbHK153168Bi-Blade Vitrectomy CutterMedical Instrument Development LaboratoriesK121675VERSAVITSynergetics, Inc.K120170PROCARE PLUS VITRECTOMY SYSTEMVisioncare Devices, Inc.K102222ULTIMATE VIT ENHAMCER (UVE)Medical Instrument Development Laboratories, 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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