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FDA 510(k)

GUM MACHINE

K-Number: K831321 · 1983-07-07

ApplicantThe Gum Machine Co.
Decision Date1983-07-07
Product CodeEFS
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

GUM MACHINE is the device name listed in this FDA 510(k) record. The listed applicant is The Gum Machine Co.. It received FDA 510(k) clearance on 1983-07-07 under 510(k) number K831321. The device is classified under product code EFS. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GUM MACHINE?

GUM MACHINE is a medical device that received FDA 510(k) clearance on 1983-07-07. The listed applicant is The Gum Machine Co.. The 510(k) number is K831321.

When did GUM MACHINE receive FDA 510(k) clearance?

GUM MACHINE received FDA 510(k) clearance on 1983-07-07, under 510(k) number K831321.

Who is the listed applicant for GUM MACHINE?

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

What is the FDA product code for GUM MACHINE?

The FDA product code for GUM MACHINE is EFS.

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Related Devices (Code: EFS)

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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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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