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FDA 510(k)

RESILIENT GUM EXERCISER

K-Number: K820979 · 1982-05-10

ApplicantMartin A. Hass, D.D.S.
Decision Date1982-05-10
Product CodeJET
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

RESILIENT GUM EXERCISER is the device name listed in this FDA 510(k) record. The listed applicant is Martin A. Hass, D.D.S.. It received FDA 510(k) clearance on 1982-05-10 under 510(k) number K820979. The device is classified under product code JET. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RESILIENT GUM EXERCISER?

RESILIENT GUM EXERCISER is a medical device that received FDA 510(k) clearance on 1982-05-10. The listed applicant is Martin A. Hass, D.D.S.. The 510(k) number is K820979.

When did RESILIENT GUM EXERCISER receive FDA 510(k) clearance?

RESILIENT GUM EXERCISER received FDA 510(k) clearance on 1982-05-10, under 510(k) number K820979.

Who is the listed applicant for RESILIENT GUM EXERCISER?

The FDA 510(k) record lists Martin A. Hass, D.D.S. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RESILIENT GUM EXERCISER?

The FDA product code for RESILIENT GUM EXERCISER is JET.

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Related Devices (Code: JET)

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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