CAMINO VENTRICULAR NEEDLE— 510(k) K920088

Name: FDA 510(k) clearance K920088
Creator: U.S. Food and Drug Administration
Published: 1992-05-01

Substantially Equivalent

Camino Laboratories, Inc.

FDA 510(k) clearance K920088 for CAMINO VENTRICULAR NEEDLE, Substantially Equivalent on 1992-05-01. Applicant: Camino Laboratories, Inc.. Device class: 1.

Clearance details

Applicant: Camino Laboratories, Inc.
Product code: Code HCD
Device class: Class 1
Regulation: 21 CFR 882.4060
Advisory panel: Neurology
Date received: 1992-01-08
Decision date: 1992-05-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Diego, CA, US

Download summary PDF View on FDA.gov ↗

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