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FDA 510(k)

VANISH II

K-Number: K833093 · 1983-12-12

ApplicantWarner-Lambert Co.
Decision Date1983-12-12
Product CodeKGO
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

VANISH II is the device name listed in this FDA 510(k) record. The listed applicant is Warner-Lambert Co.. It received FDA 510(k) clearance on 1983-12-12 under 510(k) number K833093. The device is classified under product code KGO. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VANISH II?

VANISH II is a medical device that received FDA 510(k) clearance on 1983-12-12. The listed applicant is Warner-Lambert Co.. The 510(k) number is K833093.

When did VANISH II receive FDA 510(k) clearance?

VANISH II received FDA 510(k) clearance on 1983-12-12, under 510(k) number K833093.

Who is the listed applicant for VANISH II?

The FDA 510(k) record lists Warner-Lambert Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VANISH II?

The FDA product code for VANISH II is KGO.

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Other records listing Warner-Lambert Co. as applicant

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Related Devices (Code: KGO)

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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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