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FDA 510(k)

ANA 70 DISPERSED PHASE DENTAL ALLOY -- MODIFIED

K-Number: K923384 · 1993-01-11

ApplicantL.C. Dental
Decision Date1993-01-11
Product CodeEJJ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ANA 70 DISPERSED PHASE DENTAL ALLOY -- MODIFIED is the device name listed in this FDA 510(k) record. The listed applicant is L.C. Dental. It received FDA 510(k) clearance on 1993-01-11 under 510(k) number K923384. The device is classified under product code EJJ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANA 70 DISPERSED PHASE DENTAL ALLOY -- MODIFIED?

ANA 70 DISPERSED PHASE DENTAL ALLOY -- MODIFIED is a medical device that received FDA 510(k) clearance on 1993-01-11. The listed applicant is L.C. Dental. The 510(k) number is K923384.

When did ANA 70 DISPERSED PHASE DENTAL ALLOY -- MODIFIED receive FDA 510(k) clearance?

ANA 70 DISPERSED PHASE DENTAL ALLOY -- MODIFIED received FDA 510(k) clearance on 1993-01-11, under 510(k) number K923384.

Who is the listed applicant for ANA 70 DISPERSED PHASE DENTAL ALLOY -- MODIFIED?

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

What is the FDA product code for ANA 70 DISPERSED PHASE DENTAL ALLOY -- MODIFIED?

The FDA product code for ANA 70 DISPERSED PHASE DENTAL ALLOY -- MODIFIED is EJJ.

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 L.C. Dental 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.

K935217LC DENTAL HAND INSTRUMENT

Related Devices (Code: EJJ)

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.

K053114SILVERFILDunia Perwira Manufacturing Sdn. Bhd.K051010SECURALLOY, SEPTALLOY NG 50 AND SEPTALLOY NG 70SeptodontK033434BESTALOYWe Dong Myung Dental Industrial Co., Ltd.K032152BENCO ADMIXSouthern Dental Industries, Inc.K031658BENCO SPHERICALSouthern Dental Industries, Inc.K020452HIGH SILVER CONVENTIONALAb Ardent

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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