ClearanceBrief
Company ยท US

Reciprocal Labs Corporation

FDA 510(k) clearances and medical device recalls filed under this name, 2012 to 2020. Name variants (Inc, Corp, punctuation) are merged.

10510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
CAFNebulizer (Direct Patient Interface)10

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Mar 26, 2020K192724Propeller Sensor for Symbicort
Reciprocal Labs Corporation
CAF
Aug 1, 2018K180770Propeller Sensor for Neohaler
Reciprocal Labs Corporation
CAF
Nov 1, 2016K161454Propeller Sensor Model 2015-E
Reciprocal Labs Corporation
CAF
Mar 8, 2016K152882Propeller System
Reciprocal Labs
CAF
Mar 4, 2016K152482Propeller Sensor Model 2014-R
Reciprocal Labs
CAF
Jun 19, 2015K143671Propeller Model 2014-D Sensor
Reciprocal Labs
CAF
May 15, 2015K142516Propeller System
Reciprocal Labs Corporation
CAF
Mar 5, 2015K142960Propeller System 2014-R
Reciprocal Labs
CAF
May 2, 2014K140638PROPELLER SYSTEM - MODEL 2
Reciprocal Labs Corporation
CAF
Jul 2, 2012K121609ASTHMAPOLIS SYSTEM
Reciprocal Labs Corporation
CAF

Latest recalls

DateFirm and productCodeLinked 510(k)
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