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FDA 510(k)

MINI FLOW- DENTAL FLOSS

K-Number: K844626 · 1985-01-09

ApplicantMini Floss
Decision Date1985-01-09
Product CodeJES
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MINI FLOW- DENTAL FLOSS is the device name listed in this FDA 510(k) record. The listed applicant is Mini Floss. It received FDA 510(k) clearance on 1985-01-09 under 510(k) number K844626. 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 MINI FLOW- DENTAL FLOSS?

MINI FLOW- DENTAL FLOSS is a medical device that received FDA 510(k) clearance on 1985-01-09. The listed applicant is Mini Floss. The 510(k) number is K844626.

When did MINI FLOW- DENTAL FLOSS receive FDA 510(k) clearance?

MINI FLOW- DENTAL FLOSS received FDA 510(k) clearance on 1985-01-09, under 510(k) number K844626.

Who is the listed applicant for MINI FLOW- DENTAL FLOSS?

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

What is the FDA product code for MINI FLOW- DENTAL FLOSS?

The FDA product code for MINI FLOW- DENTAL FLOSS 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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