RIWOLITH 2280— 510(k) K913487
Substantially EquivalentRichard Wolf Medical Instruments Corp.
FDA 510(k) clearance K913487 for RIWOLITH 2280, Substantially Equivalent on 1992-02-05. Applicant: Richard Wolf Medical Instruments Corp.. Device class: 2.
Clearance details
- Applicant
- Richard Wolf Medical Instruments Corp.
- Product code
- Code FFK
- Device class
- Class 2
- Regulation
- 21 CFR 876.4480
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Rosemont, IL, US
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