VESSEL DILATOR— 510(k) K840641

Unknown

Aries Medical, Inc.

FDA 510(k) clearance K840641 for VESSEL DILATOR, Unknown on 1984-02-14. Applicant: Aries Medical, Inc..

Clearance details

Applicant: Aries Medical, Inc.
Advisory panel: Unknown
Date received: 1984-02-14
Decision date: 1984-02-14
Decision: Unknown
Clearance type: Traditional
Location: Mchenry, IL, US

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