SMARTPILL GI MONITORING SYSTEM, VERSION 2.0
FDA 510(k) clearance K092342 · decided 2009-10-30
Clearance details
- K-number
- K092342
- Device name
- SMARTPILL GI MONITORING SYSTEM, VERSION 2.0
- Applicant
- The Smartpill Corporation
- Decision
- Substantially Equivalent
- Date received
- 2009-08-04
- Decision date
- 2009-10-30
- Days to decision
- 87 days
- Clearance type
- Traditional
- Product code
- NYV
- Device class
- 2
- Regulation number
- 876.1725
- Medical specialty
- Gastroenterology, Urology
- Advisory committee
- Gastroenterology, Urology
- Location
- Buffalo, NY, 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 |
|---|---|---|
| Atmo Gas Capsule System (K253569) | Atmo Biosciences, Ltd. | 2026-05-22 |
| Atmo Gas Capsule System (K250940) | Atmo Biosciences, Ltd. | 2025-06-26 |
| MotiliCap GI Monitoring System (K250493) | Anx Robotica Corporation | 2025-05-21 |
| SMARTPILL GI MONITORING SYSTEM (K053547) | The Smartpill Corporation | 2006-07-18 |
Recalls involving this device
No recalls on record reference this clearance.