SEEDLINKS, MODELS 70301, 70302, 70303
K-Number: K023210 · 2003-03-28
Advertisement
Device Summary
Frequently Asked Questions
What is the SEEDLINKS, MODELS 70301, 70302, 70303?
SEEDLINKS, MODELS 70301, 70302, 70303 is a medical device that received FDA 510(k) clearance on 2003-03-28. The listed applicant is Sourcetech Medical, LLC. The 510(k) number is K023210.
When did SEEDLINKS, MODELS 70301, 70302, 70303 receive FDA 510(k) clearance?
SEEDLINKS, MODELS 70301, 70302, 70303 received FDA 510(k) clearance on 2003-03-28, under 510(k) number K023210.
Who is the listed applicant for SEEDLINKS, MODELS 70301, 70302, 70303?
The FDA 510(k) record lists Sourcetech Medical, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SEEDLINKS, MODELS 70301, 70302, 70303?
The FDA product code for SEEDLINKS, MODELS 70301, 70302, 70303 is KXK.
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 Sourcetech Medical, 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: KXK)
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.
Advertisement