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FDA 510(k)

EMA LIV CENERA DENTAL CEMENT

K-Number: K842995 · 1984-10-30

ApplicantInt'L Corp.
Decision Date1984-10-30
Product CodeEMA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

EMA LIV CENERA DENTAL CEMENT is the device name listed in this FDA 510(k) record. The listed applicant is Int'L Corp.. It received FDA 510(k) clearance on 1984-10-30 under 510(k) number K842995. The device is classified under product code EMA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EMA LIV CENERA DENTAL CEMENT?

EMA LIV CENERA DENTAL CEMENT is a medical device that received FDA 510(k) clearance on 1984-10-30. The listed applicant is Int'L Corp.. The 510(k) number is K842995.

When did EMA LIV CENERA DENTAL CEMENT receive FDA 510(k) clearance?

EMA LIV CENERA DENTAL CEMENT received FDA 510(k) clearance on 1984-10-30, under 510(k) number K842995.

Who is the listed applicant for EMA LIV CENERA DENTAL CEMENT?

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

What is the FDA product code for EMA LIV CENERA DENTAL CEMENT?

The FDA product code for EMA LIV CENERA DENTAL CEMENT is EMA.

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 Int'L Corp. 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: EMA)

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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