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FDA 510(k)

MERCURY DENTAL

K-Number: K973548 · 1998-03-23

ApplicantAleaciones Dentales Zeyco, S.A. DE C.V.
Decision Date1998-03-23
Product CodeELY
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MERCURY DENTAL is the device name listed in this FDA 510(k) record. The listed applicant is Aleaciones Dentales Zeyco, S.A. DE C.V.. It received FDA 510(k) clearance on 1998-03-23 under 510(k) number K973548. The device is classified under product code ELY. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MERCURY DENTAL?

MERCURY DENTAL is a medical device that received FDA 510(k) clearance on 1998-03-23. The listed applicant is Aleaciones Dentales Zeyco, S.A. DE C.V.. The 510(k) number is K973548.

When did MERCURY DENTAL receive FDA 510(k) clearance?

MERCURY DENTAL received FDA 510(k) clearance on 1998-03-23, under 510(k) number K973548.

Who is the listed applicant for MERCURY DENTAL?

The FDA 510(k) record lists Aleaciones Dentales Zeyco, S.A. DE C.V. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MERCURY DENTAL?

The FDA product code for MERCURY DENTAL is ELY.

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Related Devices (Code: ELY)

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.

K093587DENTAL MERCURYDmg USA, Inc.K913814MODEL #05 ANEROID SPHYGMOMANOMETER KITNational Health-Care Equipment, Inc.K902388DENTAL-QUECKSILBER (DENTAL MERCURY)Degussa AG

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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