FIELD-LEE BRAIN BIOPSY NEEDLE— 510(k) K801760

Name: FDA 510(k) clearance K801760
Creator: U.S. Food and Drug Administration
Published: 1980-09-09

Substantially Equivalent

American V. Mueller

FDA 510(k) clearance K801760 for FIELD-LEE BRAIN BIOPSY NEEDLE, Substantially Equivalent on 1980-09-09. Applicant: American V. Mueller. Device class: 1.

Clearance details

Applicant: American V. Mueller
Product code: Code HAO
Device class: Class 1
Regulation: 21 CFR 882.4535
Advisory panel: Neurology
Date received: 1980-07-28
Decision date: 1980-09-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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