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FDA 510(k)

VANISH

K-Number: K833976 · 1984-02-04

ApplicantParke-Davis Co.
Decision Date1984-02-04
Product CodeKGO
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

VANISH is the device name listed in this FDA 510(k) record. The listed applicant is Parke-Davis Co.. It received FDA 510(k) clearance on 1984-02-04 under 510(k) number K833976. 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?

VANISH is a medical device that received FDA 510(k) clearance on 1984-02-04. The listed applicant is Parke-Davis Co.. The 510(k) number is K833976.

When did VANISH receive FDA 510(k) clearance?

VANISH received FDA 510(k) clearance on 1984-02-04, under 510(k) number K833976.

Who is the listed applicant for VANISH?

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

What is the FDA product code for VANISH?

The FDA product code for VANISH is KGO.

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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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