LUMINBOND, BONDING AND CEMENTATION SYSTEM
K-Number: K883392 · 1988-10-18
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Device Summary
Frequently Asked Questions
What is the LUMINBOND, BONDING AND CEMENTATION SYSTEM?
LUMINBOND, BONDING AND CEMENTATION SYSTEM is a medical device that received FDA 510(k) clearance on 1988-10-18. The listed applicant is Scientific Pharmaceuticals, Inc.. The 510(k) number is K883392.
When did LUMINBOND, BONDING AND CEMENTATION SYSTEM receive FDA 510(k) clearance?
LUMINBOND, BONDING AND CEMENTATION SYSTEM received FDA 510(k) clearance on 1988-10-18, under 510(k) number K883392.
Who is the listed applicant for LUMINBOND, BONDING AND CEMENTATION SYSTEM?
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 LUMINBOND, BONDING AND CEMENTATION SYSTEM?
The FDA product code for LUMINBOND, BONDING AND CEMENTATION SYSTEM is EBF.
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: EBF)
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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