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FDA 510(k)

DENTAL HANDPIECES AND ATTACHMENT

K-Number: K864922 · 1987-02-19

Decision Date1987-02-19
Product CodeEKS
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DENTAL HANDPIECES AND ATTACHMENT is the device name listed in this FDA 510(k) record. The listed applicant is E&D Dental Manufacturing Co.. It received FDA 510(k) clearance on 1987-02-19 under 510(k) number K864922. The device is classified under product code EKS. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DENTAL HANDPIECES AND ATTACHMENT?

DENTAL HANDPIECES AND ATTACHMENT is a medical device that received FDA 510(k) clearance on 1987-02-19. The listed applicant is E&D Dental Manufacturing Co.. The 510(k) number is K864922.

When did DENTAL HANDPIECES AND ATTACHMENT receive FDA 510(k) clearance?

DENTAL HANDPIECES AND ATTACHMENT received FDA 510(k) clearance on 1987-02-19, under 510(k) number K864922.

Who is the listed applicant for DENTAL HANDPIECES AND ATTACHMENT?

The FDA 510(k) record lists E&D Dental Manufacturing Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DENTAL HANDPIECES AND ATTACHMENT?

The FDA product code for DENTAL HANDPIECES AND ATTACHMENT is EKS.

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 E&D Dental Manufacturing Co. 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: EKS)

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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