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FDA 510(k)

PANASIL IMPRESSION MATERIAL

K-Number: K954281 · 1996-06-24

Decision Date1996-06-24
Product CodeELW
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PANASIL IMPRESSION MATERIAL is the device name listed in this FDA 510(k) record. The listed applicant is Roydent Dental Products, Inc.. It received FDA 510(k) clearance on 1996-06-24 under 510(k) number K954281. 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 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

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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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