COMPANY
Protaryx Medical
Timeline
- FDA FDA 510(k) clearance: Protaryx Transseptal Puncture Device (PTX2-001) — K260839, Apr 10, 2026. Applicant at approval: Protaryx Medical, Inc. source ↗
FDA records (last 2 years)
- FDA 510(k) clearance: Protaryx Transseptal Puncture Device (PTX2-001) — K260839, Apr 10, 2026. Applicant at approval: Protaryx Medical, Inc. source ↗