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FDA 510(k)

DENTAL FLOSS CARD

K-Number: K860324 · 1986-03-26

Decision Date1986-03-26
Product CodeJES
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DENTAL FLOSS CARD is the device name listed in this FDA 510(k) record. The listed applicant is Washburn Laboratories. It received FDA 510(k) clearance on 1986-03-26 under 510(k) number K860324. 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 CARD?

DENTAL FLOSS CARD is a medical device that received FDA 510(k) clearance on 1986-03-26. The listed applicant is Washburn Laboratories. The 510(k) number is K860324.

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

DENTAL FLOSS CARD received FDA 510(k) clearance on 1986-03-26, under 510(k) number K860324.

Who is the listed applicant for DENTAL FLOSS CARD?

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

What is the FDA product code for DENTAL FLOSS CARD?

The FDA product code for DENTAL FLOSS CARD 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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