PANASIL IMPRESSION MATERIAL
K-Number: K954281 · 1996-06-24
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Device Summary
Frequently Asked Questions
What is the PANASIL IMPRESSION MATERIAL?
PANASIL IMPRESSION MATERIAL is a medical device that received FDA 510(k) clearance on 1996-06-24. The listed applicant is Roydent Dental Products, Inc.. The 510(k) number is K954281.
When did PANASIL IMPRESSION MATERIAL receive FDA 510(k) clearance?
PANASIL IMPRESSION MATERIAL received FDA 510(k) clearance on 1996-06-24, under 510(k) number K954281.
Who is the listed applicant for PANASIL IMPRESSION MATERIAL?
The FDA 510(k) record lists Roydent Dental Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PANASIL IMPRESSION MATERIAL?
The FDA product code for PANASIL 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 Roydent Dental Products, Inc. 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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