CAPHOSOL ARTIFICIAL SALIVA
K-Number: K991938 · 1999-08-10
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Device Summary
Frequently Asked Questions
What is the CAPHOSOL ARTIFICIAL SALIVA?
CAPHOSOL ARTIFICIAL SALIVA is a medical device that received FDA 510(k) clearance on 1999-08-10. The listed applicant is Inpharma A.S.. The 510(k) number is K991938.
When did CAPHOSOL ARTIFICIAL SALIVA receive FDA 510(k) clearance?
CAPHOSOL ARTIFICIAL SALIVA received FDA 510(k) clearance on 1999-08-10, under 510(k) number K991938.
Who is the listed applicant for CAPHOSOL ARTIFICIAL SALIVA?
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 ARTIFICIAL SALIVA?
The FDA product code for CAPHOSOL ARTIFICIAL SALIVA 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.
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