SPINAL NEEDLE— 510(k) K960405

Substantially Equivalent

Promex, Inc.

FDA 510(k) clearance K960405 for SPINAL NEEDLE, Substantially Equivalent on 1996-02-28. Applicant: Promex, Inc..

Clearance details

Applicant: Promex, Inc.
Product code: Code MIA
Advisory panel: Anesthesiology
Date received: 1996-01-29
Decision date: 1996-02-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Indianapolis, IN, US

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