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FDA 510(k)

ACRYLIC BASE DENTURE MATERIALS

K-Number: K873738 · 1987-11-20

Decision Date1987-11-20
Product CodeEBI
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ACRYLIC BASE DENTURE MATERIALS 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 1987-11-20 under 510(k) number K873738. The device is classified under product code EBI. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACRYLIC BASE DENTURE MATERIALS?

ACRYLIC BASE DENTURE MATERIALS is a medical device that received FDA 510(k) clearance on 1987-11-20. The listed applicant is E&D Dental Manufacturing Co.. The 510(k) number is K873738.

When did ACRYLIC BASE DENTURE MATERIALS receive FDA 510(k) clearance?

ACRYLIC BASE DENTURE MATERIALS received FDA 510(k) clearance on 1987-11-20, under 510(k) number K873738.

Who is the listed applicant for ACRYLIC BASE DENTURE MATERIALS?

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 ACRYLIC BASE DENTURE MATERIALS?

The FDA product code for ACRYLIC BASE DENTURE MATERIALS is EBI.

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: EBI)

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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