MODIFIED SINGLE USE LATEX EXAMINATION GLOVES— 510(k) K900453
Substantially EquivalentPhoenix Medical Technology, Inc.
FDA 510(k) clearance K900453 for MODIFIED SINGLE USE LATEX EXAMINATION 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
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Andrews, SC, US
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