Percutaneous Nephroscope System
FDA 510(k) clearance K232370 · decided 2024-05-01
Clearance details
- K-number
- K232370
- Device name
- Percutaneous Nephroscope System
- Applicant
- Karl Storz SE & CO. KG
- Decision
- Substantially Equivalent
- Date received
- 2023-08-08
- Decision date
- 2024-05-01
- Days to decision
- 267 days
- Clearance type
- Traditional
- Product code
- FGA
- Device class
- 2
- Regulation number
- 876.1500
- Medical specialty
- Gastroenterology, Urology
- Advisory committee
- Gastroenterology, Urology
- Location
- Tuttlingen, DE
- Third-party review
- No
- Expedited review
- No
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| Record | Firm | Date |
|---|---|---|
| Schoelly Nephroscope Set, Schoelly Ultra-Mini Nephroscope Set (K151308) | Schoelly Fiberoptic GmbH | 2016-02-09 |
| GYRUS ACMI IPN-2505, INVISIO SMITH PERCUTANEOUS NEPHROSCOPE SYSTEM (K072594) | Gyrus Acmi, Inc. | 2007-12-13 |
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| KARL STORZ ENDOPYELOTOMY SET FOR ENDOSCOPIC UROLOGY PROCEDURES (K950433) | KARL STORZ Endoscopy-America, Inc. | 1995-03-15 |
| KARL STORZ ADULT & PEDIATRIC NEPHROSCOPE (K940594) | KARL STORZ Endoscopy-America, Inc. | 1994-09-09 |
| FLEXIBLE FIBER OPTIC ENDOSCOPE (K922826) | Optimed Technologies, Inc. | 1993-02-19 |
| OLYMPUS RIGID PERCUTANEOUS NEPHROSCOPE (K853486) | Olympus Corp. | 1985-09-12 |
| ACMI RIGI-FLEX NEPHORSCOPE (K791182) | American Cystocope Makers, Inc. | 1979-07-30 |
| PYELOSCOPE SYSTEM (K770729) | Richard Wolf Medical Instruments Corp. | 1977-04-28 |