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FDA 510(k)

NO FLOSS FLOSSER

K-Number: K854326 · 1986-04-23

ApplicantRgm Assoc.
Decision Date1986-04-23
Product CodeJEQ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

NO FLOSS FLOSSER is the device name listed in this FDA 510(k) record. The listed applicant is Rgm Assoc.. It received FDA 510(k) clearance on 1986-04-23 under 510(k) number K854326. The device is classified under product code JEQ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NO FLOSS FLOSSER?

NO FLOSS FLOSSER is a medical device that received FDA 510(k) clearance on 1986-04-23. The listed applicant is Rgm Assoc.. The 510(k) number is K854326.

When did NO FLOSS FLOSSER receive FDA 510(k) clearance?

NO FLOSS FLOSSER received FDA 510(k) clearance on 1986-04-23, under 510(k) number K854326.

Who is the listed applicant for NO FLOSS FLOSSER?

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

What is the FDA product code for NO FLOSS FLOSSER?

The FDA product code for NO FLOSS FLOSSER is JEQ.

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Related Devices (Code: JEQ)

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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