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FDA 510(k)

KERAVISION VACUUM RING SYSTEM

K-Number: K984540 · 1999-04-28

ApplicantKeravision, Inc.
Decision Date1999-04-28
Product CodeHNO
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

KERAVISION VACUUM RING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Keravision, Inc.. It received FDA 510(k) clearance on 1999-04-28 under 510(k) number K984540. The device is classified under product code HNO. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KERAVISION VACUUM RING SYSTEM?

KERAVISION VACUUM RING SYSTEM is a medical device that received FDA 510(k) clearance on 1999-04-28. The listed applicant is Keravision, Inc.. The 510(k) number is K984540.

When did KERAVISION VACUUM RING SYSTEM receive FDA 510(k) clearance?

KERAVISION VACUUM RING SYSTEM received FDA 510(k) clearance on 1999-04-28, under 510(k) number K984540.

Who is the listed applicant for KERAVISION VACUUM RING SYSTEM?

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

What is the FDA product code for KERAVISION VACUUM RING SYSTEM?

The FDA product code for KERAVISION VACUUM RING SYSTEM is HNO.

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Related Devices (Code: HNO)

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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