SPECTRA FORM CHROMATIC ALGINATE IMPRESSION MATERIAL
K-Number: K980965 · 1998-05-01
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Device Summary
Frequently Asked Questions
What is the SPECTRA FORM CHROMATIC ALGINATE IMPRESSION MATERIAL?
SPECTRA FORM CHROMATIC ALGINATE IMPRESSION MATERIAL is a medical device that received FDA 510(k) clearance on 1998-05-01. The listed applicant is Cavex Holland BV. The 510(k) number is K980965.
When did SPECTRA FORM CHROMATIC ALGINATE IMPRESSION MATERIAL receive FDA 510(k) clearance?
SPECTRA FORM CHROMATIC ALGINATE IMPRESSION MATERIAL received FDA 510(k) clearance on 1998-05-01, under 510(k) number K980965.
Who is the listed applicant for SPECTRA FORM CHROMATIC ALGINATE IMPRESSION MATERIAL?
The FDA 510(k) record lists Cavex Holland BV as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SPECTRA FORM CHROMATIC ALGINATE IMPRESSION MATERIAL?
The FDA product code for SPECTRA FORM CHROMATIC ALGINATE 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 Cavex Holland BV 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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