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FDA 510(k)

Lascod Impression Materials

K-Number: K201184 · 2020-05-05

ApplicantLascod Spa
Decision Date2020-05-05
Product CodeELW
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Lascod Impression Materials is the device name listed in this FDA 510(k) record. The listed applicant is Lascod Spa. It received FDA 510(k) clearance on 2020-05-05 under 510(k) number K201184. The device is classified under product code ELW. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Lascod Impression Materials?

Lascod Impression Materials is a medical device that received FDA 510(k) clearance on 2020-05-05. The listed applicant is Lascod Spa. The 510(k) number is K201184.

When did Lascod Impression Materials receive FDA 510(k) clearance?

Lascod Impression Materials received FDA 510(k) clearance on 2020-05-05, under 510(k) number K201184.

Who is the listed applicant for Lascod Impression Materials?

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

What is the FDA product code for Lascod Impression Materials?

The FDA product code for Lascod Impression Materials is ELW.

Related Devices (Code: ELW)

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.

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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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