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FDA 510(k)

CROWN & BRIDGE RESIN FOR FABRICAT/DE

K-Number: K820456 · 1982-03-19

ApplicantRohm and Haas Co.
Decision Date1982-03-19
Product CodeEBG
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CROWN & BRIDGE RESIN FOR FABRICAT/DE is the device name listed in this FDA 510(k) record. The listed applicant is Rohm and Haas Co.. It received FDA 510(k) clearance on 1982-03-19 under 510(k) number K820456. The device is classified under product code EBG. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CROWN & BRIDGE RESIN FOR FABRICAT/DE?

CROWN & BRIDGE RESIN FOR FABRICAT/DE is a medical device that received FDA 510(k) clearance on 1982-03-19. The listed applicant is Rohm and Haas Co.. The 510(k) number is K820456.

When did CROWN & BRIDGE RESIN FOR FABRICAT/DE receive FDA 510(k) clearance?

CROWN & BRIDGE RESIN FOR FABRICAT/DE received FDA 510(k) clearance on 1982-03-19, under 510(k) number K820456.

Who is the listed applicant for CROWN & BRIDGE RESIN FOR FABRICAT/DE?

The FDA 510(k) record lists Rohm and Haas Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CROWN & BRIDGE RESIN FOR FABRICAT/DE?

The FDA product code for CROWN & BRIDGE RESIN FOR FABRICAT/DE is EBG.

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.

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Other records listing Rohm and Haas 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.

K911299EQUIPMENT/MATERIAL DECONTAMINATING KITK834435CROWN & BRIDGE RESINK822722CROWN S BRIDGE RESIN

Related Devices (Code: EBG)

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.

K261261Dura-ArchHangzhou SHINING3D Dental Technology Co., Ltd.K253380“FLNT Base” and “FLNT Temp”Liaoning Upcera Co., Ltd.K251271TempFIT Temporary Crown and Bridge ResinRizhao Huge Biomaterials Company, Ltd.K243370DentaTOOTHAsiga Pty, Ltd.K243621Evoblock, PerléonEvoden Indústria Comércio Importação E ExportaçãoK243951TEMP MASTER, PMMA-based dental resinTaiwan Dental Materials Co., Ltd.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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