125 IMPLANT SEEDS, MODEL STM1251— 510(k) K991280

Name: FDA 510(k) clearance K991280
Creator: U.S. Food and Drug Administration
Published: 1999-10-20

Substantially Equivalent

Sourcetech Medical, LLC

FDA 510(k) clearance K991280 for 125 IMPLANT SEEDS, MODEL STM1251, Substantially Equivalent on 1999-10-20. Applicant: Sourcetech Medical, LLC. Device class: 2.

Clearance details

Applicant: Sourcetech Medical, LLC
Product code: Code KXK
Device class: Class 2
Regulation: 21 CFR 892.5730
Advisory panel: Radiology
Date received: 1999-04-14
Decision date: 1999-10-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Carol Stream, IL, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.