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FDA 510(k)

LIQCRYLIC PRO DENTAL RESIN

K-Number: K972573 · 1997-09-16

ApplicantDentsply Intl.
Decision Date1997-09-16
Product CodeEBI
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

LIQCRYLIC PRO DENTAL RESIN is the device name listed in this FDA 510(k) record. The listed applicant is Dentsply Intl.. It received FDA 510(k) clearance on 1997-09-16 under 510(k) number K972573. The device is classified under product code EBI. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIQCRYLIC PRO DENTAL RESIN?

LIQCRYLIC PRO DENTAL RESIN is a medical device that received FDA 510(k) clearance on 1997-09-16. The listed applicant is Dentsply Intl.. The 510(k) number is K972573.

When did LIQCRYLIC PRO DENTAL RESIN receive FDA 510(k) clearance?

LIQCRYLIC PRO DENTAL RESIN received FDA 510(k) clearance on 1997-09-16, under 510(k) number K972573.

Who is the listed applicant for LIQCRYLIC PRO DENTAL RESIN?

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

What is the FDA product code for LIQCRYLIC PRO DENTAL RESIN?

The FDA product code for LIQCRYLIC PRO DENTAL RESIN is EBI.

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Related Devices (Code: EBI)

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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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