Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

DENTAL FLOSS HOLDER

K-Number: K813248 · 1981-12-31

Decision Date1981-12-31
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 Sewon Industry. It received FDA 510(k) clearance on 1981-12-31 under 510(k) number K813248. 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 1981-12-31. The listed applicant is Sewon Industry. The 510(k) number is K813248.

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

DENTAL FLOSS HOLDER received FDA 510(k) clearance on 1981-12-31, under 510(k) number K813248.

Who is the listed applicant for DENTAL FLOSS HOLDER?

The FDA 510(k) record lists Sewon Industry 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.

Other records listing Sewon Industry 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.

View all 7 devices →

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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑