REUSABLE BRONCHIAL BIOPSY FORCEPS
FDA 510(k) clearance K022398 · decided 2002-10-11
Clearance details
- K-number
- K022398
- Device name
- REUSABLE BRONCHIAL BIOPSY FORCEPS
- Applicant
- Ballard Medical Products
- Decision
- Substantially Equivalent
- Date received
- 2002-07-23
- Decision date
- 2002-10-11
- Days to decision
- 80 days
- Clearance type
- Traditional
- Product code
- BWH
- Device class
- 2
- Regulation number
- 874.4680
- Medical specialty
- Ear, Nose, Throat
- Advisory committee
- Ear, Nose, Throat
- Location
- Draper, UT, 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 |
|---|---|---|
| Radial Jaw 4 Pulmonary Biopsy Forceps (K252921) | Boston Scientific Corporation | 2025-09-26 |
| RADIAL JAW 4 PULMONARY BIOPSY FORCEPS (K121186) | Boston Scientific Corp | 2012-05-16 |
| RADIAL JAW 4 PULMONARY STANDARD CAPACITY BIOPSY FORCEPS; RADIAL JAW 4 PULMONARY STANDARD CAPACITY BIOPSY FORCEPS WITH NE (K102336) | Boston Scientific Corporation | 2011-01-24 |
| WILTEK BIOPSY FORCEPS (K930419) | Wiltek Medical, Inc. | 1993-06-01 |
| UNIVERSAL BY RUSH-HAMPTON ARTHROSCOPIC (K843282) | Rush Hampton Industries | 1984-10-22 |
Recalls involving this device
No recalls on record reference this clearance.