P-S MEDICAL CSF ACCESS DEV 15MM/25MM— 510(k) K833822

Name: FDA 510(k) clearance K833822
Creator: U.S. Food and Drug Administration
Published: 1984-05-25

Substantially Equivalent

Pudenz-Schulte Medical Research Corp.

FDA 510(k) clearance K833822 for P-S MEDICAL CSF ACCESS DEV 15MM/25MM, Substantially Equivalent on 1984-05-25. Applicant: Pudenz-Schulte Medical Research Corp.. Device class: 2.

Clearance details

Applicant: Pudenz-Schulte Medical Research Corp.
Product code: Code LKG
Device class: Class 2
Regulation: 21 CFR 882.5550
Advisory panel: Neurology
Date received: 1983-11-02
Decision date: 1984-05-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

Download summary PDF View on FDA.gov ↗

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