C-22 PIT & FISSURE SEALANT
K-Number: K844057 · 1984-12-03
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Device Summary
Frequently Asked Questions
What is the C-22 PIT & FISSURE SEALANT?
C-22 PIT & FISSURE SEALANT is a medical device that received FDA 510(k) clearance on 1984-12-03. The listed applicant is Pentron Corp.. The 510(k) number is K844057.
When did C-22 PIT & FISSURE SEALANT receive FDA 510(k) clearance?
C-22 PIT & FISSURE SEALANT received FDA 510(k) clearance on 1984-12-03, under 510(k) number K844057.
Who is the listed applicant for C-22 PIT & FISSURE SEALANT?
The FDA 510(k) record lists Pentron Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for C-22 PIT & FISSURE SEALANT?
The FDA product code for C-22 PIT & FISSURE 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 Pentron 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: 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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