CROWN DELTA HYDROPHILIC IMPRESSION MATERIAL
K-Number: K041028 · 2004-05-14
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Device Summary
Frequently Asked Questions
What is the CROWN DELTA HYDROPHILIC IMPRESSION MATERIAL?
CROWN DELTA HYDROPHILIC IMPRESSION MATERIAL is a medical device that received FDA 510(k) clearance on 2004-05-14. The listed applicant is Crown Delta Corp.. The 510(k) number is K041028.
When did CROWN DELTA HYDROPHILIC IMPRESSION MATERIAL receive FDA 510(k) clearance?
CROWN DELTA HYDROPHILIC IMPRESSION MATERIAL received FDA 510(k) clearance on 2004-05-14, under 510(k) number K041028.
Who is the listed applicant for CROWN DELTA HYDROPHILIC IMPRESSION MATERIAL?
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 CROWN DELTA HYDROPHILIC IMPRESSION MATERIAL?
The FDA product code for CROWN DELTA HYDROPHILIC IMPRESSION MATERIAL 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.
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
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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