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FDA 510(k)

SUPRA-VIT(TM)

K-Number: K932669 · 1994-06-03

ApplicantMedical Instrument Development Laboratories, Inc.
Decision Date1994-06-03
Product CodeHQE
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

SUPRA-VIT(TM) 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 1994-06-03 under 510(k) number K932669. 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 SUPRA-VIT(TM)?

SUPRA-VIT(TM) is a medical device that received FDA 510(k) clearance on 1994-06-03. The listed applicant is Medical Instrument Development Laboratories, Inc.. The 510(k) number is K932669.

When did SUPRA-VIT(TM) receive FDA 510(k) clearance?

SUPRA-VIT(TM) received FDA 510(k) clearance on 1994-06-03, under 510(k) number K932669.

Who is the listed applicant for SUPRA-VIT(TM)?

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 SUPRA-VIT(TM)?

The FDA product code for SUPRA-VIT(TM) is HQE.

Related Clinical Trials

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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)K020911MID LABS AUTONOMOUS VIT ENHANCER (AVE)K992943VIT ENHANCERK971067DIGI-INJECTORK950287UNIVIT PROBEK934600MICRODRIVE

View all 22 devices →

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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