COPAL VARNISH
K-Number: K901049 · 1990-05-29
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Device Summary
Frequently Asked Questions
What is the COPAL VARNISH?
COPAL VARNISH is a medical device that received FDA 510(k) clearance on 1990-05-29. The listed applicant is Pulpdent Corp.. The 510(k) number is K901049.
When did COPAL VARNISH receive FDA 510(k) clearance?
COPAL VARNISH received FDA 510(k) clearance on 1990-05-29, under 510(k) number K901049.
Who is the listed applicant for COPAL VARNISH?
The FDA 510(k) record lists Pulpdent Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for COPAL VARNISH?
The FDA product code for COPAL VARNISH is LBH.
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 Pulpdent Corp. 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: LBH)
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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