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FDA 510(k)

CAPSULE DENTAL AMALGAM

K-Number: K803269 · 1981-01-15

ApplicantDentsply Intl.
Decision Date1981-01-15
Product Code
DecisionSubstantially Equivalent

Device Summary

CAPSULE DENTAL AMALGAM is the device name listed in this FDA 510(k) record. The listed applicant is Dentsply Intl.. It received FDA 510(k) clearance on 1981-01-15 under 510(k) number K803269. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CAPSULE DENTAL AMALGAM?

CAPSULE DENTAL AMALGAM is a medical device that received FDA 510(k) clearance on 1981-01-15. The listed applicant is Dentsply Intl.. The 510(k) number is K803269.

When did CAPSULE DENTAL AMALGAM receive FDA 510(k) clearance?

CAPSULE DENTAL AMALGAM received FDA 510(k) clearance on 1981-01-15, under 510(k) number K803269.

Who is the listed applicant for CAPSULE DENTAL AMALGAM?

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

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Other records listing Dentsply Intl. as applicant

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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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