WATERLASE FOR APICOECTOMY
K-Number: K022803 · 2003-02-03
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Device Summary
Frequently Asked Questions
What is the WATERLASE FOR APICOECTOMY?
WATERLASE FOR APICOECTOMY is a medical device that received FDA 510(k) clearance on 2003-02-03. The listed applicant is Biolase Technology, Inc.. The 510(k) number is K022803.
When did WATERLASE FOR APICOECTOMY receive FDA 510(k) clearance?
WATERLASE FOR APICOECTOMY received FDA 510(k) clearance on 2003-02-03, under 510(k) number K022803.
Who is the listed applicant for WATERLASE FOR APICOECTOMY?
The FDA 510(k) record lists Biolase Technology, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for WATERLASE FOR APICOECTOMY?
The FDA product code for WATERLASE FOR APICOECTOMY is MXF.
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 Biolase Technology, 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: MXF)
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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