PALACOS LV+G
K-Number: K050854 · 2005-07-07
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Device Summary
Frequently Asked Questions
What is the PALACOS LV+G?
PALACOS LV+G is a medical device that received FDA 510(k) clearance on 2005-07-07. The listed applicant is Heraeus Kulzer,GmbH. The 510(k) number is K050854.
When did PALACOS LV+G receive FDA 510(k) clearance?
PALACOS LV+G received FDA 510(k) clearance on 2005-07-07, under 510(k) number K050854.
Who is the listed applicant for PALACOS LV+G?
The FDA 510(k) record lists Heraeus Kulzer,GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PALACOS LV+G?
The FDA product code for PALACOS LV+G is LOD.
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 Heraeus Kulzer,GmbH 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: LOD)
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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