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FDA 510(k)

ALLOY, AMALGAM, DISP. CAPSULE

K-Number: K781242 · 1978-08-21

ApplicantLee Pharmaceuticals
Decision Date1978-08-21
Product CodeEJJ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ALLOY, AMALGAM, DISP. CAPSULE is the device name listed in this FDA 510(k) record. The listed applicant is Lee Pharmaceuticals. It received FDA 510(k) clearance on 1978-08-21 under 510(k) number K781242. 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 ALLOY, AMALGAM, DISP. CAPSULE?

ALLOY, AMALGAM, DISP. CAPSULE is a medical device that received FDA 510(k) clearance on 1978-08-21. The listed applicant is Lee Pharmaceuticals. The 510(k) number is K781242.

When did ALLOY, AMALGAM, DISP. CAPSULE receive FDA 510(k) clearance?

ALLOY, AMALGAM, DISP. CAPSULE received FDA 510(k) clearance on 1978-08-21, under 510(k) number K781242.

Who is the listed applicant for ALLOY, AMALGAM, DISP. CAPSULE?

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

What is the FDA product code for ALLOY, AMALGAM, DISP. CAPSULE?

The FDA product code for ALLOY, AMALGAM, DISP. CAPSULE is EJJ.

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Other records listing Lee Pharmaceuticals 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.

K924378RESTOBOND 4K912256PRECISE(R) BETA QUARTZ GLASS-CERAMIC INSERTK900809LEE-FISCHER CERAMIC REINFORCED PLASTIC BRACKETSK894315RESTOBOND 3/DENTIN-ENAMEL BONDING AGENTK881903PROSTHODENT VLK873123LEE COMPOSITE INLAY SYSTEM

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Related Devices (Code: EJJ)

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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

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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