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FDA 510(k)

LIFESTAT 1600 PRINTER

K-Number: K881346 · 1988-06-09

ApplicantPhysio-Control Corp.
Decision Date1988-06-09
Product CodeDSF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

LIFESTAT 1600 PRINTER 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 1988-06-09 under 510(k) number K881346. 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 LIFESTAT 1600 PRINTER?

LIFESTAT 1600 PRINTER is a medical device that received FDA 510(k) clearance on 1988-06-09. The listed applicant is Physio-Control Corp.. The 510(k) number is K881346.

When did LIFESTAT 1600 PRINTER receive FDA 510(k) clearance?

LIFESTAT 1600 PRINTER received FDA 510(k) clearance on 1988-06-09, under 510(k) number K881346.

Who is the listed applicant for LIFESTAT 1600 PRINTER?

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 LIFESTAT 1600 PRINTER?

The FDA product code for LIFESTAT 1600 PRINTER is DSF.

Related Clinical Trials

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.

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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)

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.

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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