DERLIN— 510(k) K964817
Substantially EquivalentDerlin Company , Ltd.
FDA 510(k) clearance K964817 for DERLIN, Substantially Equivalent on 1997-01-24. Applicant: Derlin Company , Ltd.. Device class: 1.
Clearance details
- Applicant
- Derlin Company , 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
- Ming Sheng E. Rd. Taipei, TW
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More clearances from Derlin Company , Ltd.
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