SEWON DENTAL FLOSSER
K-Number: K870996 · 1987-03-19
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Device Summary
Frequently Asked Questions
What is the SEWON DENTAL FLOSSER?
SEWON DENTAL FLOSSER is a medical device that received FDA 510(k) clearance on 1987-03-19. The listed applicant is Sewon Industry. The 510(k) number is K870996.
When did SEWON DENTAL FLOSSER receive FDA 510(k) clearance?
SEWON DENTAL FLOSSER received FDA 510(k) clearance on 1987-03-19, under 510(k) number K870996.
Who is the listed applicant for SEWON DENTAL FLOSSER?
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 FLOSSER?
The FDA product code for SEWON DENTAL FLOSSER 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.
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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