MODIFICATION TO SANARUS CENTRICA CORE TISSUE BIOPSY
K-Number: K022879 · 2002-09-23
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Device Summary
Frequently Asked Questions
What is the MODIFICATION TO SANARUS CENTRICA CORE TISSUE BIOPSY?
MODIFICATION TO SANARUS CENTRICA CORE TISSUE BIOPSY is a medical device that received FDA 510(k) clearance on 2002-09-23. The listed applicant is Sanarus Medical, Inc.. The 510(k) number is K022879.
When did MODIFICATION TO SANARUS CENTRICA CORE TISSUE BIOPSY receive FDA 510(k) clearance?
MODIFICATION TO SANARUS CENTRICA CORE TISSUE BIOPSY received FDA 510(k) clearance on 2002-09-23, under 510(k) number K022879.
Who is the listed applicant for MODIFICATION TO SANARUS CENTRICA CORE TISSUE BIOPSY?
The FDA 510(k) record lists Sanarus Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MODIFICATION TO SANARUS CENTRICA CORE TISSUE BIOPSY?
The FDA product code for MODIFICATION TO SANARUS CENTRICA CORE TISSUE BIOPSY is KNW.
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 Sanarus Medical, 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: KNW)
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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