DEGUFILL (TM) WHIT-SEALANT
K-Number: K902742 · 1990-09-12
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Device Summary
Frequently Asked Questions
What is the DEGUFILL (TM) WHIT-SEALANT?
DEGUFILL (TM) WHIT-SEALANT is a medical device that received FDA 510(k) clearance on 1990-09-12. The listed applicant is Degussa AG. The 510(k) number is K902742.
When did DEGUFILL (TM) WHIT-SEALANT receive FDA 510(k) clearance?
DEGUFILL (TM) WHIT-SEALANT received FDA 510(k) clearance on 1990-09-12, under 510(k) number K902742.
Who is the listed applicant for DEGUFILL (TM) WHIT-SEALANT?
The FDA 510(k) record lists Degussa AG as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DEGUFILL (TM) WHIT-SEALANT?
The FDA product code for DEGUFILL (TM) WHIT-SEALANT is EBC.
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 Degussa AG 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: EBC)
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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