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FDA 510(k)

ULTIMATE VIT ENHAMCER (UVE)

K-Number: K102222 · 2011-04-08

ApplicantMedical Instrument Development Laboratories, Inc.
Decision Date2011-04-08
Product CodeHQE
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

ULTIMATE VIT ENHAMCER (UVE) is the device name listed in this FDA 510(k) record. The listed applicant is Medical Instrument Development Laboratories, Inc.. It received FDA 510(k) clearance on 2011-04-08 under 510(k) number K102222. 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 ULTIMATE VIT ENHAMCER (UVE)?

ULTIMATE VIT ENHAMCER (UVE) is a medical device that received FDA 510(k) clearance on 2011-04-08. The listed applicant is Medical Instrument Development Laboratories, Inc.. The 510(k) number is K102222.

When did ULTIMATE VIT ENHAMCER (UVE) receive FDA 510(k) clearance?

ULTIMATE VIT ENHAMCER (UVE) received FDA 510(k) clearance on 2011-04-08, under 510(k) number K102222.

Who is the listed applicant for ULTIMATE VIT ENHAMCER (UVE)?

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

What is the FDA product code for ULTIMATE VIT ENHAMCER (UVE)?

The FDA product code for ULTIMATE VIT ENHAMCER (UVE) is HQE.

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Other records listing Medical Instrument Development Laboratories, 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.

K020911MID LABS AUTONOMOUS VIT ENHANCER (AVE)K992943VIT ENHANCERK971067DIGI-INJECTORK950287UNIVIT PROBEK934600MICRODRIVEK932669SUPRA-VIT(TM)

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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.K033390COLIBRI DISPOSABLE VITRECTOMY CUTTERMicroworld Medical Instruments, 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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