PALACOS R
K-Number: K030902 · 2003-09-23
Advertisement
Device Summary
Frequently Asked Questions
What is the PALACOS R?
PALACOS R is a medical device that received FDA 510(k) clearance on 2003-09-23. The listed applicant is Heraeus Kulzer GmbH & Co. KG. The 510(k) number is K030902.
When did PALACOS R receive FDA 510(k) clearance?
PALACOS R received FDA 510(k) clearance on 2003-09-23, under 510(k) number K030902.
Who is the listed applicant for PALACOS R?
The FDA 510(k) record lists Heraeus Kulzer GmbH & Co. KG as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PALACOS R?
The FDA product code for PALACOS R 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 & Co. KG 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.
Advertisement