GALILEOS FAMILY
K-Number: K123070 · 2013-03-15
Advertisement
Device Summary
Frequently Asked Questions
What is the GALILEOS FAMILY?
GALILEOS FAMILY is a medical device that received FDA 510(k) clearance on 2013-03-15. The listed applicant is Sirona Dental Systems GmbH. The 510(k) number is K123070.
When did GALILEOS FAMILY receive FDA 510(k) clearance?
GALILEOS FAMILY received FDA 510(k) clearance on 2013-03-15, under 510(k) number K123070.
Who is the listed applicant for GALILEOS FAMILY?
The FDA 510(k) record lists Sirona Dental Systems GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GALILEOS FAMILY?
The FDA product code for GALILEOS FAMILY is OAS.
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 Sirona Dental Systems 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: OAS)
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