ClearanceBrief
Company ยท US

Echo Ultrasound

FDA 510(k) clearances and medical device recalls filed under this name, 1985 to 1993. Name variants (Inc, Corp, punctuation) are merged.

6510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
DQCPhonocardiograph1
DXKEchocardiograph1
DYOBand, Material, Orthodontic1
GXXBlock, Test, Ultrasonic Scanner Calibration1
IYOSystem, Imaging, Pulsed Echo, Ultrasonic1
JOTElectrode, Gel, Electrosurgical1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Jan 22, 1993K924054PHONOCARDIOGRAPH
Echo Ultrasound
DQC
Sep 19, 1990K903414TRANSESOPHAGEAL PROBE HOLDER & DISINFECTING COLUMN
Echo Ultrasound
DXK
Oct 12, 1989K893225COUPLANT WARMING DEVICE
Echo Ultrasound
IYO
Aug 3, 1987K872519STERILIZED OMNI GEL
Echo Ultrasound
JOT
Jan 23, 1985K844120ULTRASONIC SCANNER CALIBRATION & TEST OBJECTS
Echo Ultrasound
GXX
Jan 23, 1985K844034SONOCARE
Echo Ultrasound
DYO

Latest recalls

DateFirm and productCodeLinked 510(k)
No recalls in this window.
Get alerts for these product codes