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FDA 510(k)

MULTITOME MODEL 1000, VITRECTOMY DRIVING SYSTEM

K-Number: K911998 · 1991-07-26

ApplicantAllergan Medical Optics
Decision Date1991-07-26
Product CodeHQE
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

MULTITOME MODEL 1000, VITRECTOMY DRIVING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Allergan Medical Optics. It received FDA 510(k) clearance on 1991-07-26 under 510(k) number K911998. 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 MULTITOME MODEL 1000, VITRECTOMY DRIVING SYSTEM?

MULTITOME MODEL 1000, VITRECTOMY DRIVING SYSTEM is a medical device that received FDA 510(k) clearance on 1991-07-26. The listed applicant is Allergan Medical Optics. The 510(k) number is K911998.

When did MULTITOME MODEL 1000, VITRECTOMY DRIVING SYSTEM receive FDA 510(k) clearance?

MULTITOME MODEL 1000, VITRECTOMY DRIVING SYSTEM received FDA 510(k) clearance on 1991-07-26, under 510(k) number K911998.

Who is the listed applicant for MULTITOME MODEL 1000, VITRECTOMY DRIVING SYSTEM?

The FDA 510(k) record lists Allergan Medical Optics as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MULTITOME MODEL 1000, VITRECTOMY DRIVING SYSTEM?

The FDA product code for MULTITOME MODEL 1000, VITRECTOMY DRIVING SYSTEM is HQE.

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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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