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FDA 510(k)

DENTAL FLOSS HOLDER

K-Number: K821155 · 1982-05-24

ApplicantEric L. Smith
Decision Date1982-05-24
Product CodeJES
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DENTAL FLOSS HOLDER is the device name listed in this FDA 510(k) record. The listed applicant is Eric L. Smith. It received FDA 510(k) clearance on 1982-05-24 under 510(k) number K821155. The device is classified under product code JES. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DENTAL FLOSS HOLDER?

DENTAL FLOSS HOLDER is a medical device that received FDA 510(k) clearance on 1982-05-24. The listed applicant is Eric L. Smith. The 510(k) number is K821155.

When did DENTAL FLOSS HOLDER receive FDA 510(k) clearance?

DENTAL FLOSS HOLDER received FDA 510(k) clearance on 1982-05-24, under 510(k) number K821155.

Who is the listed applicant for DENTAL FLOSS HOLDER?

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

What is the FDA product code for DENTAL FLOSS HOLDER?

The FDA product code for DENTAL FLOSS HOLDER 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.

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

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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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