VITRABOND LIGHT CURE GLASS IONOMER LINER
K-Number: K882821 · 1988-09-15
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Device Summary
Frequently Asked Questions
What is the VITRABOND LIGHT CURE GLASS IONOMER LINER?
VITRABOND LIGHT CURE GLASS IONOMER LINER is a medical device that received FDA 510(k) clearance on 1988-09-15. The listed applicant is 3M Company. The 510(k) number is K882821.
When did VITRABOND LIGHT CURE GLASS IONOMER LINER receive FDA 510(k) clearance?
VITRABOND LIGHT CURE GLASS IONOMER LINER received FDA 510(k) clearance on 1988-09-15, under 510(k) number K882821.
Who is the listed applicant for VITRABOND LIGHT CURE GLASS IONOMER LINER?
The FDA 510(k) record lists 3M Company as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VITRABOND LIGHT CURE GLASS IONOMER LINER?
The FDA product code for VITRABOND LIGHT CURE GLASS IONOMER LINER is EKJ.
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 3M Company 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: EKJ)
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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