Vsm(R) R2 Paper Chart Recorder

FDA 510(k) K880554 · Physio-Control Corp.

Substantially Equivalent

510(k) numberK880554

Submission

Device name
Vsm(R) R2 Paper Chart Recorder
Applicant
Physio-Control Corp.
Redmond, WA, US
Received
February 9, 1988
Decision date
May 6, 1988
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

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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

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Questions and answers

When was Vsm(R) R2 Paper Chart Recorder cleared by the FDA?

Vsm(R) R2 Paper Chart Recorder (K880554) received a 510(k) decision of Substantially Equivalent on May 6, 1988, 87 days after the submission was received.

What is the product code of K880554?

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