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FDA 510(k)

POWER OPERATED AND CONTROLLED VITREOUS SCISSORS

K-Number: K891601 · 1989-05-23

ApplicantMira, Inc.
Decision Date1989-05-23
Product CodeHQE
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

POWER OPERATED AND CONTROLLED VITREOUS SCISSORS is the device name listed in this FDA 510(k) record. The listed applicant is Mira, Inc.. It received FDA 510(k) clearance on 1989-05-23 under 510(k) number K891601. 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 POWER OPERATED AND CONTROLLED VITREOUS SCISSORS?

POWER OPERATED AND CONTROLLED VITREOUS SCISSORS is a medical device that received FDA 510(k) clearance on 1989-05-23. The listed applicant is Mira, Inc.. The 510(k) number is K891601.

When did POWER OPERATED AND CONTROLLED VITREOUS SCISSORS receive FDA 510(k) clearance?

POWER OPERATED AND CONTROLLED VITREOUS SCISSORS received FDA 510(k) clearance on 1989-05-23, under 510(k) number K891601.

Who is the listed applicant for POWER OPERATED AND CONTROLLED VITREOUS SCISSORS?

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

What is the FDA product code for POWER OPERATED AND CONTROLLED VITREOUS SCISSORS?

The FDA product code for POWER OPERATED AND CONTROLLED VITREOUS SCISSORS is HQE.

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Other records listing Mira, Inc. as applicant

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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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