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FDA 510(k)

QUIK COMBO

K-Number: K943301 · 1995-02-03

ApplicantPhysio-Control Corp.
Decision Date1995-02-03
Product CodeDRX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

QUIK COMBO 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 1995-02-03 under 510(k) number K943301. The device is classified under product code DRX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QUIK COMBO?

QUIK COMBO is a medical device that received FDA 510(k) clearance on 1995-02-03. The listed applicant is Physio-Control Corp.. The 510(k) number is K943301.

When did QUIK COMBO receive FDA 510(k) clearance?

QUIK COMBO received FDA 510(k) clearance on 1995-02-03, under 510(k) number K943301.

Who is the listed applicant for QUIK COMBO?

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 QUIK COMBO?

The FDA product code for QUIK COMBO is DRX.

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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: DRX)

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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