STARION UNIVERSAL POWER SUPPLY— 510(k) K070871

Name: FDA 510(k) clearance K070871
Creator: U.S. Food and Drug Administration
Published: 2007-04-13

Substantially Equivalent

Starion Instruments

FDA 510(k) clearance K070871 for STARION UNIVERSAL POWER SUPPLY, Substantially Equivalent on 2007-04-13. Applicant: Starion Instruments. Device class: 2.

Clearance details

Applicant: Starion Instruments
Product code: Code HQO
Device class: Class 2
Regulation: 21 CFR 886.4115
Advisory panel: Ophthalmic
Date received: 2007-03-29
Decision date: 2007-04-13
Decision: Substantially Equivalent
Clearance type: Special
Location: Sunnyvale, CA, US

Download summary PDF View on FDA.gov ↗

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K971538 — MENTOR GEMINI HEMOSTATIC ERASER1997-07-14
K962135 — D.O.R.C. MICRODIATHERMY SYSTEM1996-08-29

More clearances from Starion Instruments

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K062257 — STARION INSTRUMENTS THERMAL LITIGATING SHEARS2006-10-10
K050308 — THERMAL CAUTERY PROBE2005-02-25
K002547 — STARION INSTRUMENTS POWER POINT CAUTERY GRASPER/DISSECTOR2000-10-20
K001262 — THERMAL CAUTERY FORCEPS2000-06-14
K001273 — STARION INSTRUMENTS POWER POINT CAUTERY CLAMP2000-06-14

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