PROVISO
K-Number: K041886 · 2004-08-04
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Device Summary
Frequently Asked Questions
What is the PROVISO?
PROVISO is a medical device that received FDA 510(k) clearance on 2004-08-04. The listed applicant is Scientific Pharmaceuticals, Inc.. The 510(k) number is K041886.
When did PROVISO receive FDA 510(k) clearance?
PROVISO received FDA 510(k) clearance on 2004-08-04, under 510(k) number K041886.
Who is the listed applicant for PROVISO?
The FDA 510(k) record lists Scientific Pharmaceuticals, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PROVISO?
The FDA product code for PROVISO is EBG.
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 Scientific Pharmaceuticals, Inc. 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: EBG)
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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