K233020 is an FDA 510(k) clearance for the TauTona Pneumoperitoneum Assist Device (TPAD). This device is classified as a Insufflator, Laparoscopic (Class II - Special Controls, product code HIF).
Submitted by Tautona Group Research & Development, Co., LLC (Redwood City, US). The FDA issued a Cleared decision on January 12, 2024, 112 days after receiving the submission on September 22, 2023.
This device falls under the Obstetrics & Gynecology FDA review panel. Regulated under 21 CFR 884.1730.
| 510(k) Number | K233020 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | September 22, 2023 |
| Decision Date | January 12, 2024 |
| Days to Decision | 112 days |
| Submission Type | Traditional |
| Review Panel | Obstetrics & Gynecology (OB) |
| Summary | Summary PDF |
| Product Code | HIF - Insufflator, Laparoscopic |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 884.1730 |