Graseby Pcas Model No. 0124-0701, PVS Dytinhr Pump
FDA 510(k) K865051 · Panamedix, Inc.
510(k) numberK865051
Submission
- Device name
- Graseby Pcas Model No. 0124-0701, PVS Dytinhr Pump
- Applicant
- Panamedix, Inc.
Costa Mesa, CA, US - Received
- December 24, 1986
- Decision date
- February 10, 1987
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- FRN – Pump, Infusion
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 880.5725
- Specialty
- General Hospital
Other 510(k)s with product code FRN
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K253703 | RemunityPRO+ Pump for Remodulin® (treprostinil) InjectionFRN · Traditional | Deka R&D Corp | 07/24/2026SE |
| K252015 | FreedomEdge Infusion System; High-Flo SubQ Needle Set; Precision Flow Rate TubingFRN · Traditional | Koru Medical Systems, Inc. | 01/28/2026SE |
| K251640 | SIGMA Spectrum Infusion Pump with Master Drug LibraryFRN · Traditional | Baxter Healthcare Corporation | 07/28/2025SE |
| K251636 | Spectrum IQ Infusion System with Dose IQ Safety Software (3570009)FRN · Traditional | Baxter Healthcare Corporation | 07/28/2025SE |
| K242752 | MRidium 3870 MRI Infusion Pump System (3870)FRN · Traditional | Iradimed Corporation | 05/28/2025SE |
| K243855 | BD Alaris Infusion System with Guardrails Suite MXFRN · Traditional | Carefusion 303, Inc. | 04/25/2025SE |
| K242115 | Plum Duo Precision IV PumpFRN · Traditional | Icu Medical, Inc. | 04/02/2025SE |
| K242114 | Plum Solo Precision IV PumpFRN · Traditional | Icu Medical, Inc. | 04/02/2025SE |
| K250357 | RemunityPRO Pump for Remodulin® (treprostinil) InjectionFRN · Special | Deka Research & Development Corp. | 03/11/2025SE |
| K241736 | Remunity 2.0 Pump for Remodulin (treprostinil) InjectionFRN · Traditional | Deka Research and Development Corp. | 01/16/2025SE |
More from Deka Research and Development Corp.
| 510(k) | Device | Decision |
|---|---|---|
| K871848 | Nutrition Delivery Sets for VM 05 Ambula. PumpKNT · Traditional | 02/03/1988SE |
| K871843 | Two Fluid W/Check ValveFPA · Traditional | 07/21/1987SE |
| K871842 | Two Fluid I.V. SetsFPA · Traditional | 06/24/1987SE |
| K871841 | Three Fluid I.V. SetsFPA · Traditional | 06/24/1987SE |
| K864395 | Low Volume Extension SetFPK · Traditional | 12/16/1986SE |
Questions and answers
When was Graseby Pcas Model No. 0124-0701, PVS Dytinhr Pump cleared by the FDA?
Graseby Pcas Model No. 0124-0701, PVS Dytinhr Pump (K865051) received a 510(k) decision of Substantially Equivalent on February 10, 1987, 48 days after the submission was received.
What is the product code of K865051?
The FDA product code is FRN – Pump, Infusion, a Class II (moderate risk) device regulated under 21 CFR 880.5725.