Cardiocommand Inc.
3 FDA 510(k) clearances · Recalling firm
| Record | Firm | Date |
|---|---|---|
| ***REF #200***TAPSCOPE 550. Each pouch contains one (1) 18 French esophageal stethoscope w recall (Z-0071-2012) | Cardiocommand Inc. | 2011-10-19 |
| ***REF #250***TAPSCOPE 550F. Each pouch contains one (1) 18 French esophageal stethoscope recall (Z-0072-2012) | Cardiocommand Inc. | 2011-10-19 |
| The device is labeled as AMS TAPSYSTEM Model 2A Esophageal Pulse generator (used in the Op recall (Z-0568-04) | Cardiocommand Inc. | 2004-07-20 |
Track Cardiocommand Inc. automatically
Every clearance here is in the API, with alerts when new ones post.