PATIENT EXAMINATION GLOVE (POWDERED)— 510(k) K954293
Substantially EquivalentMedline Products Co. , Ltd.
FDA 510(k) clearance K954293 for PATIENT EXAMINATION GLOVE (POWDERED), Substantially Equivalent on 1996-07-26. Applicant: Medline Products Co. , Ltd.. Device class: 1.
Clearance details
- Applicant
- Medline Products Co. , Ltd.
- 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
- Songkhla, TH
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Data sourced from openFDA. This site is unofficial and independent of the FDA.