AESCULAP NEURO PATTIES, NEUROSORB 4, 6, AND 75 (GREEN & WHITE)— 510(k) K031008

Name: FDA 510(k) clearance K031008
Creator: U.S. Food and Drug Administration
Published: 2003-05-09

Substantially Equivalent

Aesculap

FDA 510(k) clearance K031008 for AESCULAP NEURO PATTIES, NEUROSORB 4, 6, AND 75 (GREEN & WHITE), Substantially Equivalent on 2003-05-09. Applicant: Aesculap. Device class: 2.

Clearance details

Applicant: Aesculap
Product code: Product code HBA
Device class: Class 2
Regulation: 21 CFR 882.4700
Advisory panel: Neurology
Date received: 2003-03-31
Decision date: 2003-05-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Center Valley, PA, US

Download summary PDF View on FDA.gov ↗

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K121822 — DELICOT2012-09-10
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K062085 — S4 SPINAL SYSTEM2007-03-02
K062510 — AESCULAP STERILCONTAINER SYSTEM2006-11-17
K061135 — MINOP DISPOSABLE INTRODUCER 10F, MODEL ME010; 19F, MODEL ME0192006-07-11
K043079 — BICONTACT HIP SYSTEM WITH U-CAP2004-12-08

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