NEXTSTEP RETROGRADE
FDA 510(k) clearance K130192 · decided 2013-05-10
Clearance details
- K-number
- K130192
- Device name
- NEXTSTEP RETROGRADE
- Applicant
- Arrow International, Inc.
- Decision
- Unknown
- Date received
- 2013-01-25
- Decision date
- 2013-05-10
- Days to decision
- 105 days
- Clearance type
- Traditional
- Product code
- MSD
- Device class
- 2
- Regulation number
- 876.5540
- Medical specialty
- Gastroenterology, Urology
- Advisory committee
- Gastroenterology, Urology
- Location
- Reading, PA, US
- Third-party review
- No
- Expedited review
- No
+ Add to Predicate Builder ◉ Watch Arrow International
Need this as data, not a web page?
Query all 176,000+ clearances through the Atlas FDA API, or subscribe to weekly change alerts. Self-serve from $29/mo.
Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
Recalls involving this device
No recalls on record reference this clearance.