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FDA 510(k)

MENTOR ADVENT A/B SYSTEM

K-Number: K960765 · 1996-08-08

ApplicantMentor Ophthalmics, Inc.
Decision Date1996-08-08
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MENTOR ADVENT A/B SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Mentor Ophthalmics, Inc.. It received FDA 510(k) clearance on 1996-08-08 under 510(k) number K960765. The device is classified under product code IYO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MENTOR ADVENT A/B SYSTEM?

MENTOR ADVENT A/B SYSTEM is a medical device that received FDA 510(k) clearance on 1996-08-08. The listed applicant is Mentor Ophthalmics, Inc.. The 510(k) number is K960765.

When did MENTOR ADVENT A/B SYSTEM receive FDA 510(k) clearance?

MENTOR ADVENT A/B SYSTEM received FDA 510(k) clearance on 1996-08-08, under 510(k) number K960765.

Who is the listed applicant for MENTOR ADVENT A/B SYSTEM?

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

What is the FDA product code for MENTOR ADVENT A/B SYSTEM?

The FDA product code for MENTOR ADVENT A/B SYSTEM is IYO.

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Other records listing Mentor Ophthalmics, 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.

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Related Devices (Code: IYO)

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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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