PROPHYPEARLS
K-Number: K031868 · 2003-07-09
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Device Summary
Frequently Asked Questions
What is the PROPHYPEARLS?
PROPHYPEARLS is a medical device that received FDA 510(k) clearance on 2003-07-09. The listed applicant is Kavo America. The 510(k) number is K031868.
When did PROPHYPEARLS receive FDA 510(k) clearance?
PROPHYPEARLS received FDA 510(k) clearance on 2003-07-09, under 510(k) number K031868.
Who is the listed applicant for PROPHYPEARLS?
The FDA 510(k) record lists Kavo America as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PROPHYPEARLS?
The FDA product code for PROPHYPEARLS is EFB.
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 Kavo America 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: EFB)
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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