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FDA 510(k)

SEWON DENTAL FLOSS FOLDER

K-Number: K842846 · 1984-08-17

Decision Date1984-08-17
Product CodeJES
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SEWON DENTAL FLOSS FOLDER is the device name listed in this FDA 510(k) record. The listed applicant is Sewon Industry. It received FDA 510(k) clearance on 1984-08-17 under 510(k) number K842846. 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 SEWON DENTAL FLOSS FOLDER?

SEWON DENTAL FLOSS FOLDER is a medical device that received FDA 510(k) clearance on 1984-08-17. The listed applicant is Sewon Industry. The 510(k) number is K842846.

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

SEWON DENTAL FLOSS FOLDER received FDA 510(k) clearance on 1984-08-17, under 510(k) number K842846.

Who is the listed applicant for SEWON DENTAL FLOSS FOLDER?

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 SEWON DENTAL FLOSS FOLDER?

The FDA product code for SEWON DENTAL FLOSS FOLDER 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.

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