SIASCOPE V
K-Number: K062736 · 2007-09-14
Advertisement
Device Summary
Frequently Asked Questions
What is the SIASCOPE V?
SIASCOPE V is a medical device that received FDA 510(k) clearance on 2007-09-14. The listed applicant is Astron Clinica Limited. The 510(k) number is K062736.
When did SIASCOPE V receive FDA 510(k) clearance?
SIASCOPE V received FDA 510(k) clearance on 2007-09-14, under 510(k) number K062736.
Who is the listed applicant for SIASCOPE V?
The FDA 510(k) record lists Astron Clinica Limited as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SIASCOPE V?
The FDA product code for SIASCOPE V is PSN.
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 Astron Clinica Limited 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: PSN)
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