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FDA 510(k)

LIFESTAT 200

K-Number: K831232 · 1983-07-28

ApplicantPhysio-Control Corp.
Decision Date1983-07-28
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

LIFESTAT 200 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 1983-07-28 under 510(k) number K831232. The device is classified under product code DXN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIFESTAT 200?

LIFESTAT 200 is a medical device that received FDA 510(k) clearance on 1983-07-28. The listed applicant is Physio-Control Corp.. The 510(k) number is K831232.

When did LIFESTAT 200 receive FDA 510(k) clearance?

LIFESTAT 200 received FDA 510(k) clearance on 1983-07-28, under 510(k) number K831232.

Who is the listed applicant for LIFESTAT 200?

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 200?

The FDA product code for LIFESTAT 200 is DXN.

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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: DXN)

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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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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