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FDA 510(k)

CHECK-UP PLAQUE FIGHTING GUM

K-Number: K860843 · 1986-05-21

Decision Date1986-05-21
Product CodeEJR
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CHECK-UP PLAQUE FIGHTING GUM is the device name listed in this FDA 510(k) record. The listed applicant is Minnetonka, Inc.. It received FDA 510(k) clearance on 1986-05-21 under 510(k) number K860843. The device is classified under product code EJR. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CHECK-UP PLAQUE FIGHTING GUM?

CHECK-UP PLAQUE FIGHTING GUM is a medical device that received FDA 510(k) clearance on 1986-05-21. The listed applicant is Minnetonka, Inc.. The 510(k) number is K860843.

When did CHECK-UP PLAQUE FIGHTING GUM receive FDA 510(k) clearance?

CHECK-UP PLAQUE FIGHTING GUM received FDA 510(k) clearance on 1986-05-21, under 510(k) number K860843.

Who is the listed applicant for CHECK-UP PLAQUE FIGHTING GUM?

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

What is the FDA product code for CHECK-UP PLAQUE FIGHTING GUM?

The FDA product code for CHECK-UP PLAQUE FIGHTING GUM is EJR.

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 Minnetonka, Inc. 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: EJR)

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

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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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