Angioscopy Pump
FDA 510(k) K895074 · Baxter Healthcare Corp
510(k) numberK895074
Submission
- Device name
- Angioscopy Pump
- Applicant
- Baxter Healthcare Corp
Santa Ana, CA, US - Received
- August 14, 1989
- Decision date
- January 31, 1990
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- DQI – Withdrawal/Infusion Pump
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 870.1800
- Specialty
- Cardiovascular
Other 510(k)s with product code DQI
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K960486 | Ksea Model 383320 20 AngiomatDQI · Traditional | Karl Storz Endoscopy | 10/25/1996SE |
| K935763 | SurgipumpDQI · Traditional | W.O.M. World of Medicine GmbH | 04/21/1994SE |
| K922541 | Usci Super 9 Ptca Guiding CatheterDQI · Traditional | C.R. Bard, Inc. | 12/08/1992SE |
| K924110 | Leocor Corflo Pump -- ModificationDQI · Traditional | Leocor, Inc. | 09/01/1992SE |
| K905189 | Baxter Angioscopy Pump Tubing Set (Model NL)DQI · Traditional | Baxter Healthcare Corp | 01/30/1991SE |
| K902444 | Clearview(Tm) Angioscopic Irrigation PumpDQI · Traditional | Intramed Laboratories, Inc. | 08/30/1990SE |
| K895688 | Nobles-Lai Engineering Infusion PumpDQI · Traditional | Nobles-Lai Engineering, Inc. | 02/26/1990SE |
| K871422 | Olympus Angioscopy PumpDQI · Traditional | Olympus Corp. | 08/12/1987SE |
More from Olympus Corp.
| 510(k) | Device | Decision |
|---|---|---|
| K251745 | Welch Allyn FlexiPort Blood Pressure Cuffs (FlexiPort Blood Pressure Cuffs)DXQ · Traditional | 12/16/2025SE |
| K251640 | SIGMA Spectrum Infusion Pump with Master Drug LibraryFRN · Traditional | 07/28/2025SE |
| K251636 | Spectrum IQ Infusion System with Dose IQ Safety Software (3570009)FRN · Traditional | 07/28/2025SE |
| K243529 | Solution Administration SetsFPA · Traditional | 03/14/2025SE |
| K242339 | Intravascular Extension Sets and AccessoriesFPA · Traditional | 02/28/2025SE |
| K242390 | Novum IQ Syringe Pump (40800BAXUS)FRN · Special | 09/05/2024SE |
| K241564 | Actifuse ABX; Actifuse MIS; Actifuse Shape; ALTAPORE; ALTAPORE SHAPE; ALTAPORE MISMQV · Traditional | 08/02/2024SE |
| K230665 | Dose IQ Safety SoftwarePHC · Traditional | 03/29/2024SE |
| K211122 | Novum IQ Large Volume PumpFRN · Traditional | 03/29/2024SE |
| K231849 | MiniCap Extended Life PD Transfer Set with Twist Clamp - Code 5C4482A; MiniCap Extended…KDJ · Traditional | 03/12/2024SE |
Questions and answers
When was Angioscopy Pump cleared by the FDA?
Angioscopy Pump (K895074) received a 510(k) decision of Substantially Equivalent on January 31, 1990, 170 days after the submission was received.
What is the product code of K895074?
The FDA product code is DQI – Withdrawal/Infusion Pump, a Class II (moderate risk) device regulated under 21 CFR 870.1800.