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FDA 510(k)

VSM(R) R2 PAPER CHART RECORDER

K-Number: K880554 · 1988-05-06

ApplicantPhysio-Control Corp.
Decision Date1988-05-06
Product CodeDSF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

VSM(R) R2 PAPER CHART RECORDER is the device name listed in this FDA 510(k) record. The listed applicant is Physio-Control Corp.. It received FDA 510(k) clearance on 1988-05-06 under 510(k) number K880554. The device is classified under product code DSF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VSM(R) R2 PAPER CHART RECORDER?

VSM(R) R2 PAPER CHART RECORDER is a medical device that received FDA 510(k) clearance on 1988-05-06. The listed applicant is Physio-Control Corp.. The 510(k) number is K880554.

When did VSM(R) R2 PAPER CHART RECORDER receive FDA 510(k) clearance?

VSM(R) R2 PAPER CHART RECORDER received FDA 510(k) clearance on 1988-05-06, under 510(k) number K880554.

Who is the listed applicant for VSM(R) R2 PAPER CHART RECORDER?

The FDA 510(k) record lists Physio-Control Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VSM(R) R2 PAPER CHART RECORDER?

The FDA product code for VSM(R) R2 PAPER CHART RECORDER is DSF.

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Other records listing Physio-Control Corp. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K991910LIFEPAK 12 BIPHASICK990338NIBP AND CO2 OPTIONS FOR THE PHYSIO-CONTROL LIFEPAK 12 DEFIBRILLATOR/MONITOR SYSTEMK983393LIFEPAK 500 BIPHASICK973486LIFE PAK 12K962359LIFEPAK 300K955854LIFEPAK 500

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Related Devices (Code: DSF)

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K910871EDENTEC DIGITAL CHARTER MODEL 3710Edentec Corp.K912929DASH IVAstro-Med, Inc.K905856MODEL 556 MONITORGe Medical Systems Information TechnologiesK902586GRI LASERGRAPH(TM) ECG PAPERGri Medical Products, Inc.K902230COLORADO COLOR IMAGING RECORDERHoneywell, Inc.K901385GABRIEL MEDICAL CLS THERMAL RECORDERGabriel Medical, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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