FDA 510(k) Applications Submitted by Pressure Products Medical Device Manufacturing LLC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K241042 | 04/17/2024 | SafeSharp Transseptal Needle (CLICK071, CLICK171, CLICK098, CLICK198) | Pressure Products Medical Device Manufacturing LLC. |
| K221707 | 06/13/2022 | SafeSept« Transseptal Guidewire (SS-140) | Pressure Products Medical Device Manufacturing LLC. |
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