QuantaFlo
FDA 510(k) K143094 · Semler Scientific, Inc.
510(k) numberK143094
Submission
- Device name
- QuantaFlo
- Applicant
- Semler Scientific, Inc.
Portland, OR, US - Received
- October 28, 2014
- Decision date
- March 5, 2015
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- JOM – Plethysmograph, Photoelectric, Pneumatic Or Hydraulic
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 870.2780
- Specialty
- Cardiovascular
Other 510(k)s with product code JOM
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K220527 | PADnet XpressJOM · Special | Collaborative Care Diagnostics, LLC, D.B.A.… | 10/20/2022SE |
| K213730 | MESI mTABLET TBI diagnostic system, MESI mTABLET TBIJOM · Traditional | Mesi, Development of Medical Devices, Ltd.; Mesi… | 04/21/2022SE |
| K200567 | ASI Plethysmogrpah AnalyzerJOM · Traditional | Arterial Stiffness, Inc. | 02/26/2021SE |
| K201046 | Automated ankle brachial pressure index measuring device, MESI mTABLET systemJOM · Traditional | Mesi D.O.O.; Mesi, Development of Medical… | 12/11/2020SE |
| K191266 | VitalScan ANSJOM · Traditional | Medeia, Inc. | 01/15/2020SE |
| K172655 | Automated ankle brachial pressure index measuring deviceJOM · Traditional | Mesi D.O.O.; Mesi, Development of Medical… | 01/11/2018SE |
| K173696 | TBL-ABI SystemJOM · Special | Ld Technology, LLC | 12/19/2017SE |
| K143152 | TM-ABI systemJOM · Traditional | Ld Technology, LLC | 07/22/2015SE |
| K123921 | Bodytronic 200JOM · Traditional | Bauerfeind AG | 04/26/2013SE |
| K121108 | Dopplex AbilityJOM · Traditional | Huntleigh Healthcare | 01/03/2013SE |
Questions and answers
When was QuantaFlo cleared by the FDA?
QuantaFlo (K143094) received a 510(k) decision of Substantially Equivalent on March 5, 2015, 128 days after the submission was received.
What is the product code of K143094?
The FDA product code is JOM – Plethysmograph, Photoelectric, Pneumatic Or Hydraulic, a Class II (moderate risk) device regulated under 21 CFR 870.2780.