A10 Ultrascope Recorder

FDA 510(k) K890142 · Ems Medical, Inc.

Substantially Equivalent

510(k) numberK890142

Submission

Device name
A10 Ultrascope Recorder
Applicant
Ems Medical, Inc.
Livermore, CA, US
Received
January 13, 1989
Decision date
February 6, 1989
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
DSF – Recorder, Paper Chart
Device class
Class I (low risk)
Regulation
21 CFR 870.2810
Specialty
Cardiovascular

Other 510(k)s with product code DSF

510(k)DeviceApplicantDecision
K910871Edentec Digital Charter Model 3710DSF · Traditional Edentec Corp.08/29/1991SE
K912929Dash IVDSF · Traditional Astro-Med, Inc.08/13/1991SE
K905856Model 556 MonitorDSF · Traditional Ge Medical Systems Information Technologies01/11/1991SE
K902586Gri Lasergraph(Tm) ECG PaperDSF · Traditional Gri Medical Products, Inc.06/22/1990SE
K902230Colorado Color Imaging RecorderDSF · Traditional Honeywell, Inc.06/19/1990SE
K901385Gabriel Medical CLS Thermal RecorderDSF · Traditional Gabriel Medical, Inc.05/09/1990SE
K895111Type 9541 Recorder, Paper ChartDSF · Traditional S & W Medico Teknik01/26/1990SE
K894922WR3500 and WR3600 Series RecordersDSF · Traditional Western Graphtec01/26/1990SE
K894736MT96000 Paper Chart RecorderDSF · Traditional Astro-Med, Inc.12/13/1989SE
K894607PAQ10 Paper Chart RecorderDSF · Traditional Protocol Systems, Inc.10/26/1989SE

More from Protocol Systems, Inc.

510(k)DeviceDecision
K896306Glove N GelLYY · Traditional 12/11/1989SE

Questions and answers

When was A10 Ultrascope Recorder cleared by the FDA?

A10 Ultrascope Recorder (K890142) received a 510(k) decision of Substantially Equivalent on February 6, 1989, 24 days after the submission was received.

What is the product code of K890142?

The FDA product code is DSF – Recorder, Paper Chart, a Class I (low risk) device regulated under 21 CFR 870.2810.