AESCULAP NEURO PATTIES— 510(k) K062406

Substantially Equivalent

Aesculap, Inc.

FDA 510(k) clearance K062406 for AESCULAP NEURO PATTIES, Substantially Equivalent on 2006-09-15. Applicant: Aesculap, Inc.. Device class: 2.

Clearance details

Applicant: Aesculap, Inc.
Product code: Code HBA
Device class: Class 2
Regulation: 21 CFR 882.4700
Advisory panel: Neurology
Date received: 2006-08-17
Decision date: 2006-09-15
Decision: Substantially Equivalent
Clearance type: Special
Location: Center Valley, PA, 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.