K242374 is an FDA 510(k) clearance for the ULSPIRA TS™ Nitric Oxide Therapy System. This device is classified as a Apparatus, Nitric Oxide Delivery (Class II - Special Controls, product code MRN).
Submitted by Airgas Therapeutics, LLC (Plumsteadville, US). The FDA issued a Cleared decision on January 17, 2025, 161 days after receiving the submission on August 9, 2024.
This device falls under the Anesthesiology FDA review panel. Regulated under 21 CFR 868.5165.
| 510(k) Number | K242374 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | August 09, 2024 |
| Decision Date | January 17, 2025 |
| Days to Decision | 161 days |
| Submission Type | Special |
| Review Panel | Anesthesiology (AN) |
| Summary | Summary PDF |
| Product Code | MRN - Apparatus, Nitric Oxide Delivery |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 868.5165 |