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FDA 510(k)

ENVOY AND VISTA BRITE TIP

K-Number: K000715 · 2000-03-31

ApplicantCordis Corp.
Decision Date2000-03-31
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ENVOY AND VISTA BRITE TIP is the device name listed in this FDA 510(k) record. The listed applicant is Cordis Corp.. It received FDA 510(k) clearance on 2000-03-31 under 510(k) number K000715. The device is classified under product code DQY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENVOY AND VISTA BRITE TIP?

ENVOY AND VISTA BRITE TIP is a medical device that received FDA 510(k) clearance on 2000-03-31. The listed applicant is Cordis Corp.. The 510(k) number is K000715.

When did ENVOY AND VISTA BRITE TIP receive FDA 510(k) clearance?

ENVOY AND VISTA BRITE TIP received FDA 510(k) clearance on 2000-03-31, under 510(k) number K000715.

Who is the listed applicant for ENVOY AND VISTA BRITE TIP?

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

What is the FDA product code for ENVOY AND VISTA BRITE TIP?

The FDA product code for ENVOY AND VISTA BRITE TIP is DQY.

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Other records listing Cordis Corp. 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: DQY)

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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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