SWISS LITHOCLAST MASTER HANDPIECE AND 3.2 MM PROBE— 510(k) K974164
Substantially EquivalentMedical Device Consultants, Inc.
FDA 510(k) clearance K974164 for SWISS LITHOCLAST MASTER HANDPIECE AND 3.2 MM PROBE, Substantially Equivalent on 1997-12-18. Applicant: Medical Device Consultants, Inc.. Device class: 2.
Clearance details
- Applicant
- Medical Device Consultants, Inc.
- 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
- North Attleboro, MA, US
Recent devices under product code FFK
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