MODIFIED LOW POWDER SINGLE USE LATEX EXAM GLOVES— 510(k) K900454

Substantially Equivalent

Phoenix Medical Technology, Inc.

FDA 510(k) clearance K900454 for MODIFIED LOW POWDER SINGLE USE LATEX EXAM GLOVES, Substantially Equivalent on 1990-02-13. Applicant: Phoenix Medical Technology, Inc..

Clearance details

Applicant: Phoenix Medical Technology, Inc.
Product code: Code LYY
Advisory panel: General Hospital
Date received: 1990-01-30
Decision date: 1990-02-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Andrews, SC, US

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