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FDA 510(k)

COTTON TIPPED POINT

K-Number: K780929 · 1978-06-30

Decision Date1978-06-30
Product CodeKXF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

COTTON TIPPED POINT is the device name listed in this FDA 510(k) record. The listed applicant is Young Dental Manufacturing Co. 1, LLC. It received FDA 510(k) clearance on 1978-06-30 under 510(k) number K780929. The device is classified under product code KXF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COTTON TIPPED POINT?

COTTON TIPPED POINT is a medical device that received FDA 510(k) clearance on 1978-06-30. The listed applicant is Young Dental Manufacturing Co. 1, LLC. The 510(k) number is K780929.

When did COTTON TIPPED POINT receive FDA 510(k) clearance?

COTTON TIPPED POINT received FDA 510(k) clearance on 1978-06-30, under 510(k) number K780929.

Who is the listed applicant for COTTON TIPPED POINT?

The FDA 510(k) record lists Young Dental Manufacturing Co. 1, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for COTTON TIPPED POINT?

The FDA product code for COTTON TIPPED POINT is KXF.

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 Young Dental Manufacturing Co. 1, LLC 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 16 devices →

Related Devices (Code: KXF)

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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