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FDA 510(k)

MODEL 1051, MONITOR

K-Number: K790328 · 1979-03-02

ApplicantApplied Medical Research
Decision Date1979-03-02
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODEL 1051, MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Applied Medical Research. It received FDA 510(k) clearance on 1979-03-02 under 510(k) number K790328. 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 MODEL 1051, MONITOR?

MODEL 1051, MONITOR is a medical device that received FDA 510(k) clearance on 1979-03-02. The listed applicant is Applied Medical Research. The 510(k) number is K790328.

When did MODEL 1051, MONITOR receive FDA 510(k) clearance?

MODEL 1051, MONITOR received FDA 510(k) clearance on 1979-03-02, under 510(k) number K790328.

Who is the listed applicant for MODEL 1051, MONITOR?

The FDA 510(k) record lists Applied Medical Research as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODEL 1051, MONITOR?

The FDA product code for MODEL 1051, MONITOR is DXN.

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Other records listing Applied Medical Research 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.

K800025DINAMAP RESEARCH MONITOR 1245K791580CEREBRAL FUNCTION MONITOR 870K791159DINAMAP MODEL 855K790322OPTIONAL ACCESSORY FOOT SWITCH MODEL 100K782073DINAMAP MODELS 1160 AND 1165K781053DINAMAP MODEL 846

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Related Devices (Code: DXN)

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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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