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FDA 510(k)

EYE SYS VISTA

K-Number: K973756 · 1997-11-13

ApplicantEyesys Technologies, Inc.
Decision Date1997-11-13
Product CodeHLQ
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

EYE SYS VISTA is the device name listed in this FDA 510(k) record. The listed applicant is Eyesys Technologies, Inc.. It received FDA 510(k) clearance on 1997-11-13 under 510(k) number K973756. The device is classified under product code HLQ. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EYE SYS VISTA?

EYE SYS VISTA is a medical device that received FDA 510(k) clearance on 1997-11-13. The listed applicant is Eyesys Technologies, Inc.. The 510(k) number is K973756.

When did EYE SYS VISTA receive FDA 510(k) clearance?

EYE SYS VISTA received FDA 510(k) clearance on 1997-11-13, under 510(k) number K973756.

Who is the listed applicant for EYE SYS VISTA?

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

What is the FDA product code for EYE SYS VISTA?

The FDA product code for EYE SYS VISTA is HLQ.

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Related Devices (Code: HLQ)

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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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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