Intravascular Imaging System/Modified
FDA 510(k) K910281 · Intertherapy, Inc.
510(k) numberK910281
Submission
- Device name
- Intravascular Imaging System/Modified
- Applicant
- Intertherapy, Inc.
Santa Ana, CA, US - Received
- January 23, 1991
- Decision date
- May 13, 1991
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- JOP – Transducer, Ultrasonic
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 870.2880
- Specialty
- Cardiovascular
Other 510(k)s with product code JOP
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|---|---|---|---|
| K242662 | Falcon/Xpress (Falcon/Xpress)JOP · Traditional | Viasonix , Ltd. | 12/18/2024SE |
| K233976 | VasoGuard (V10, V8, V6, V4, V2)JOP · Traditional | Corvascular Diagnostics, LLC | 07/19/2024SE |
| K153762 | Smartdop XT6JOP · Traditional | Koven Technology, Inc. | 05/25/2016SE |
| K131623 | Smartdop XTJOP · Traditional | Koven Technology, Inc. | 01/17/2014SE |
| K131860 | Vasculab VL4000 Photoplethysmograph with Pulse Volume RecordingJOP · Traditional | Us Vascular, LLC | 09/27/2013SE |
| K111416 | FalconJOP · Traditional | Viasonix , Ltd. | 07/15/2011SE |
| K071730 | Studiodop VicorderJOP · Abbreviated | Skidmore Medical, Limited | 12/20/2007SE |
| K010482 | Echoflow Portable Doppler Blood Flow Measurement System; Model PEF-1JOP · Special | Echocath, Inc. | 03/20/2001SE |
| K002766 | Nicolet VasoguardJOP · Abbreviated | Nicolet Biomedical | 11/30/2000SE |
| K990642 | Echoflow Doppler Blood Velocity MeterJOP · Traditional | Echocath, Inc. | 09/16/1999SE |
More from Echocath, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K913763 | Interpret(Tm) Catheter Linear TranslatorLYK · Traditional | 11/20/1991SE |
| K912600 | Interpret(Tm) Intravascular Imaging CatheterITX · Traditional | 11/19/1991SE |
| K900305 | Intravascular Imaging SystemsLYK · Traditional | 04/20/1990SE |
| K895159 | Intravascular Imaging SystemLYK · Traditional | 03/12/1990SE |
Questions and answers
When was Intravascular Imaging System/Modified cleared by the FDA?
Intravascular Imaging System/Modified (K910281) received a 510(k) decision of Substantially Equivalent on May 13, 1991, 110 days after the submission was received.
What is the product code of K910281?
The FDA product code is JOP – Transducer, Ultrasonic, a Class II (moderate risk) device regulated under 21 CFR 870.2880.