TELEDYNE GETZ BARRIER-DENTIN SEALER
K-Number: K852756 · 1985-07-31
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Device Summary
Frequently Asked Questions
What is the TELEDYNE GETZ BARRIER-DENTIN SEALER?
TELEDYNE GETZ BARRIER-DENTIN SEALER is a medical device that received FDA 510(k) clearance on 1985-07-31. The listed applicant is Scientific Pharmaceuticals, Inc.. The 510(k) number is K852756.
When did TELEDYNE GETZ BARRIER-DENTIN SEALER receive FDA 510(k) clearance?
TELEDYNE GETZ BARRIER-DENTIN SEALER received FDA 510(k) clearance on 1985-07-31, under 510(k) number K852756.
Who is the listed applicant for TELEDYNE GETZ BARRIER-DENTIN SEALER?
The FDA 510(k) record lists Scientific Pharmaceuticals, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TELEDYNE GETZ BARRIER-DENTIN SEALER?
The FDA product code for TELEDYNE GETZ BARRIER-DENTIN SEALER 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 Scientific Pharmaceuticals, Inc. 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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