STORZ MODULITH (TM) LITHOTRIPTER
FDA premarket approval P920051/S001 · decided 1995-12-19
Approval details
- PMA number
- P920051
- Supplement
- S001
- Supplement type
- Normal 180 Day Track
- Supplement reason
- Change Design/Components/Specifications/Material
- Trade name
- STORZ MODULITH (TM) LITHOTRIPTER
- Applicant
- KARL STORZ Endoscopy-America, Inc.
- Date received
- 1995-07-24
- Decision date
- 1995-12-19
- Days to decision
- 148 days
- Decision code
- APRL
- Advisory committee
- Gastroenterology, Urology
- Expedited review
- No
- Location
- Kennesaw, GA
- Statement
- APPROVAL FOR AMOBILE VERSION OF THE STORZ MODULITH LITHOTRIPTER, MODEL SL20
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