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FDA 510(k)

VES-10 INTRAOCULAR SCISSORS DRIVE

K-Number: K864035 · 1986-12-15

ApplicantTrek Medical Products, Inc.
Decision Date1986-12-15
Product CodeHQE
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

VES-10 INTRAOCULAR SCISSORS DRIVE is the device name listed in this FDA 510(k) record. The listed applicant is Trek Medical Products, Inc.. It received FDA 510(k) clearance on 1986-12-15 under 510(k) number K864035. 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 VES-10 INTRAOCULAR SCISSORS DRIVE?

VES-10 INTRAOCULAR SCISSORS DRIVE is a medical device that received FDA 510(k) clearance on 1986-12-15. The listed applicant is Trek Medical Products, Inc.. The 510(k) number is K864035.

When did VES-10 INTRAOCULAR SCISSORS DRIVE receive FDA 510(k) clearance?

VES-10 INTRAOCULAR SCISSORS DRIVE received FDA 510(k) clearance on 1986-12-15, under 510(k) number K864035.

Who is the listed applicant for VES-10 INTRAOCULAR SCISSORS DRIVE?

The FDA 510(k) record lists Trek Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VES-10 INTRAOCULAR SCISSORS DRIVE?

The FDA product code for VES-10 INTRAOCULAR SCISSORS DRIVE is HQE.

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Other records listing Trek Medical Products, Inc. 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.

K920937COMPUTERIZED PUPILK920944FTS-200 GAS SYSTEMK900808RAPID AUTOMATIC PNEUMOPERITONEUM-IK902784FIBER OPTIC LIGHT SOURCEK895813GLAUCOMA MECHANICAL TREPHINEK882403OPHTHALMIC FLUID INJECTOR

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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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