Reciprocal Labs Corporation is one of 13451 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Reciprocal Labs Corporation - FDA 510(k) Cleared Devices
Recent clearances: Propeller Sensor for Symbicort, Propeller Sensor for Neohaler, Propeller Sensor Model 2015-E
6
Total
6
Cleared
0
Denied
Reciprocal Labs Corporation has 6 FDA 510(k) cleared medical devices. Based in Madison, US.
Historical record: 6 cleared submissions from 2012 to 2020. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Reciprocal Labs Corporation Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Reciprocal Labs Corporation
6 devices
Cleared
Mar 26, 2020
Propeller Sensor for Symbicort
Anesthesiology
181d
Cleared
Aug 01, 2018
Propeller Sensor for Neohaler
Anesthesiology
131d
Cleared
Nov 01, 2016
Propeller Sensor Model 2015-E
Anesthesiology
159d
Cleared
May 15, 2015
Propeller System
Anesthesiology
249d
Cleared
May 02, 2014
PROPELLER SYSTEM - MODEL 2
Anesthesiology
51d
Cleared
Jul 02, 2012
ASTHMAPOLIS SYSTEM
Anesthesiology
31d