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FDA 510(k)

ENTRAVISION MODECO II VITREOUS CUTTING HANDPIECE

K-Number: K870775 · 1987-03-26

ApplicantEntravision, Inc.
Decision Date1987-03-26
Product CodeHQE
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

ENTRAVISION MODECO II VITREOUS CUTTING HANDPIECE is the device name listed in this FDA 510(k) record. The listed applicant is Entravision, Inc.. It received FDA 510(k) clearance on 1987-03-26 under 510(k) number K870775. 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 ENTRAVISION MODECO II VITREOUS CUTTING HANDPIECE?

ENTRAVISION MODECO II VITREOUS CUTTING HANDPIECE is a medical device that received FDA 510(k) clearance on 1987-03-26. The listed applicant is Entravision, Inc.. The 510(k) number is K870775.

When did ENTRAVISION MODECO II VITREOUS CUTTING HANDPIECE receive FDA 510(k) clearance?

ENTRAVISION MODECO II VITREOUS CUTTING HANDPIECE received FDA 510(k) clearance on 1987-03-26, under 510(k) number K870775.

Who is the listed applicant for ENTRAVISION MODECO II VITREOUS CUTTING HANDPIECE?

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

What is the FDA product code for ENTRAVISION MODECO II VITREOUS CUTTING HANDPIECE?

The FDA product code for ENTRAVISION MODECO II VITREOUS CUTTING HANDPIECE is HQE.

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Other records listing Entravision, 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.

K862063ENTRAVISION MODECO II I/A MACHINE & I/A HANDPIECEK862064ENTRAVISION EP-500 I/A ECCO PACK

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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