Narcotrace 40 - NT40

FDA 510(k) K833656 · Narco Bio-Systems

Substantially Equivalent

510(k) numberK833656

Submission

Device name
Narcotrace 40 - NT40
Applicant
Narco Bio-Systems
Mchenry, IL, US
Received
October 20, 1983
Decision date
May 9, 1984
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
K853683UMS-100FAP · Traditional 01/10/1986SE
K832869Motility Measurement Sys MMS-100FFX · Traditional 10/31/1983SE
K813502Narco Telecare Isoflo Pressure MonitorDRS · Traditional 12/29/1981SE
K811376Ultrasonic QFM System 1000DPW · Traditional 08/13/1981SE
K810431Narco Tlecare Miniature Pressure DomeDRS · Traditional 03/11/1981SE
K801544Porta-Fib LPDLDD · Traditional 07/14/1980SE
K760084Monitor, GSR (NB-401)HCC · Traditional 07/26/1976SE
K760083Physioscope · Traditional 07/20/1976SE

Questions and answers

When was Narcotrace 40 - NT40 cleared by the FDA?

Narcotrace 40 - NT40 (K833656) received a 510(k) decision of Substantially Equivalent on May 9, 1984, 202 days after the submission was received.

What is the product code of K833656?

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