CAPHOSOL
K-Number: K030802 · 2003-11-25
Advertisement
Device Summary
Frequently Asked Questions
What is the CAPHOSOL?
CAPHOSOL is a medical device that received FDA 510(k) clearance on 2003-11-25. The listed applicant is Inpharma A.S.. The 510(k) number is K030802.
When did CAPHOSOL receive FDA 510(k) clearance?
CAPHOSOL received FDA 510(k) clearance on 2003-11-25, under 510(k) number K030802.
Who is the listed applicant for CAPHOSOL?
The FDA 510(k) record lists Inpharma A.S. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CAPHOSOL?
The FDA product code for CAPHOSOL is LFD.
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 Inpharma A.S. 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: LFD)
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