MODIFIED LOW POWDER SINGLE USE LATEX EXAM GLOVES— 510(k) K900454
Substantially EquivalentPhoenix 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.. Device class: 1.
Clearance details
- Applicant
- Phoenix Medical Technology, Inc.
- Product code
- Code LYY
- Device class
- Class 1
- Regulation
- 21 CFR 880.6250
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Andrews, SC, US
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