PATIENT EXAMINATION GLOVEWS— 510(k) K913531
Substantially EquivalentPt. Sarana Indoprotex
FDA 510(k) clearance K913531 for PATIENT EXAMINATION GLOVEWS, Substantially Equivalent on 1992-01-07. Applicant: Pt. Sarana Indoprotex. Device class: 1.
Clearance details
- Applicant
- Pt. Sarana Indoprotex
- 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
- Lampung 35001-Iodonesia, IO
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More clearances from Pt. Sarana Indoprotex
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