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FDA 510(k)

IMPRESSION MATERIAL, DENTAL SILICON RTV

K-Number: K760231 · 1976-07-21

Decision Date1976-07-21
Product CodeELW
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

IMPRESSION MATERIAL, DENTAL SILICON RTV is the device name listed in this FDA 510(k) record. The listed applicant is Crown Delta Corp.. It received FDA 510(k) clearance on 1976-07-21 under 510(k) number K760231. 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 IMPRESSION MATERIAL, DENTAL SILICON RTV?

IMPRESSION MATERIAL, DENTAL SILICON RTV is a medical device that received FDA 510(k) clearance on 1976-07-21. The listed applicant is Crown Delta Corp.. The 510(k) number is K760231.

When did IMPRESSION MATERIAL, DENTAL SILICON RTV receive FDA 510(k) clearance?

IMPRESSION MATERIAL, DENTAL SILICON RTV received FDA 510(k) clearance on 1976-07-21, under 510(k) number K760231.

Who is the listed applicant for IMPRESSION MATERIAL, DENTAL SILICON RTV?

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

What is the FDA product code for IMPRESSION MATERIAL, DENTAL SILICON RTV?

The FDA product code for IMPRESSION MATERIAL, DENTAL SILICON RTV is ELW.

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 Crown Delta 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.

View all 18 devices →

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.

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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