VUTLER G.U.M. WITH FLUORIDE
K-Number: K952091 · 1995-06-28
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Device Summary
Frequently Asked Questions
What is the VUTLER G.U.M. WITH FLUORIDE?
VUTLER G.U.M. WITH FLUORIDE is a medical device that received FDA 510(k) clearance on 1995-06-28. The listed applicant is John O. Butler Co.. The 510(k) number is K952091.
When did VUTLER G.U.M. WITH FLUORIDE receive FDA 510(k) clearance?
VUTLER G.U.M. WITH FLUORIDE received FDA 510(k) clearance on 1995-06-28, under 510(k) number K952091.
Who is the listed applicant for VUTLER G.U.M. WITH FLUORIDE?
The FDA 510(k) record lists John O. Butler Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VUTLER G.U.M. WITH FLUORIDE?
The FDA product code for VUTLER G.U.M. WITH FLUORIDE is JES.
Related Clinical Trials
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.
Other records listing John O. Butler Co. 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.
Related Devices (Code: JES)
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.
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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