KARL STORZ BOUGIES AND DILATORS
FDA 510(k) clearance K950125 · decided 1995-02-07
Clearance details
- K-number
- K950125
- Device name
- KARL STORZ BOUGIES AND DILATORS
- Applicant
- KARL STORZ Endoscopy-America, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1995-01-12
- Decision date
- 1995-02-07
- Days to decision
- 26 days
- Clearance type
- Traditional
- Product code
- FAX
- Device class
- 1
- Regulation number
- 876.5520
- Medical specialty
- Gastroenterology, Urology
- Advisory committee
- Gastroenterology, Urology
- Location
- Culver City, CA, US
- Third-party review
- No
- Expedited review
- No
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Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
| Record | Firm | Date |
|---|---|---|
| ANTI-MIST, ANTI-FOG EYEGLASS & DENTAL (K822711) | Parker Laboratories, Inc. | 1982-11-03 |
Recalls involving this device
No recalls on record reference this clearance.
PMA approvals by this applicant
| Record | Firm | Date |
|---|---|---|
| Photodynamic Diagnostic D-Light C System (P050027/S036) | KARL STORZ Endoscopy-America, Inc. | 2026-07-21 |
| Photodynamic Diagnostic D-Light C (PDD) System (P050027/S035) | KARL STORZ Endoscopy-America, Inc. | 2026-02-26 |
| Photodynamic Diagnostic D-Light C System (P050027/S034) | KARL STORZ Endoscopy-America, Inc. | 2025-10-01 |
| KARL STORZ Photodynamic Diagnostic D-Light C (PDD) System (P050027/S033) | KARL STORZ Endoscopy-America, Inc. | 2025-05-02 |
| KARL STORZ Photodynamic Diagnostic D-Light C (PDD) System (P050027/S032) | KARL STORZ Endoscopy-America, Inc. | 2024-09-27 |
| KARL STORZ D-Light C PDD System (P050027/S031) | KARL STORZ Endoscopy-America, Inc. | 2023-05-05 |
| KARL STORZ D-Light C PDD System (P050027/S030) | KARL STORZ Endoscopy-America, Inc. | 2022-03-17 |
| KARL STORZ D-Light C PDD System (P050027/S028) | KARL STORZ Endoscopy-America, Inc. | 2022-02-04 |