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FDA 510(k)

MID LABS AUTONOMOUS VIT ENHANCER (AVE)

K-Number: K020911 · 2002-04-29

ApplicantMedical Instrument Development Laboratories, Inc.
Decision Date2002-04-29
Product CodeHQE
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

MID LABS AUTONOMOUS VIT ENHANCER (AVE) 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 2002-04-29 under 510(k) number K020911. 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 MID LABS AUTONOMOUS VIT ENHANCER (AVE)?

MID LABS AUTONOMOUS VIT ENHANCER (AVE) is a medical device that received FDA 510(k) clearance on 2002-04-29. The listed applicant is Medical Instrument Development Laboratories, Inc.. The 510(k) number is K020911.

When did MID LABS AUTONOMOUS VIT ENHANCER (AVE) receive FDA 510(k) clearance?

MID LABS AUTONOMOUS VIT ENHANCER (AVE) received FDA 510(k) clearance on 2002-04-29, under 510(k) number K020911.

Who is the listed applicant for MID LABS AUTONOMOUS VIT ENHANCER (AVE)?

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 MID LABS AUTONOMOUS VIT ENHANCER (AVE)?

The FDA product code for MID LABS AUTONOMOUS VIT ENHANCER (AVE) 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.

K102222ULTIMATE VIT ENHAMCER (UVE)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.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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