MAMMOTOME BIOPSY SYSTEM FOR MOLECULAR IMAGING
K-Number: K093899 · 2010-04-29
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Device Summary
Frequently Asked Questions
What is the MAMMOTOME BIOPSY SYSTEM FOR MOLECULAR IMAGING?
MAMMOTOME BIOPSY SYSTEM FOR MOLECULAR IMAGING is a medical device that received FDA 510(k) clearance on 2010-04-29. The listed applicant is Ethicon Endo-Surgery, LLC. The 510(k) number is K093899.
When did MAMMOTOME BIOPSY SYSTEM FOR MOLECULAR IMAGING receive FDA 510(k) clearance?
MAMMOTOME BIOPSY SYSTEM FOR MOLECULAR IMAGING received FDA 510(k) clearance on 2010-04-29, under 510(k) number K093899.
Who is the listed applicant for MAMMOTOME BIOPSY SYSTEM FOR MOLECULAR IMAGING?
The FDA 510(k) record lists Ethicon Endo-Surgery, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MAMMOTOME BIOPSY SYSTEM FOR MOLECULAR IMAGING?
The FDA product code for MAMMOTOME BIOPSY SYSTEM FOR MOLECULAR IMAGING 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 Ethicon Endo-Surgery, LLC 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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