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FDA 510(k)

MONITOR, DINMAP, MODEL 850

K-Number: K771931 · 1977-10-27

ApplicantApplied Medical Research
Decision Date1977-10-27
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MONITOR, DINMAP, MODEL 850 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 1977-10-27 under 510(k) number K771931. 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 MONITOR, DINMAP, MODEL 850?

MONITOR, DINMAP, MODEL 850 is a medical device that received FDA 510(k) clearance on 1977-10-27. The listed applicant is Applied Medical Research. The 510(k) number is K771931.

When did MONITOR, DINMAP, MODEL 850 receive FDA 510(k) clearance?

MONITOR, DINMAP, MODEL 850 received FDA 510(k) clearance on 1977-10-27, under 510(k) number K771931.

Who is the listed applicant for MONITOR, DINMAP, MODEL 850?

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 MONITOR, DINMAP, MODEL 850?

The FDA product code for MONITOR, DINMAP, MODEL 850 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 100K790328MODEL 1051, MONITORK782073DINAMAP MODELS 1160 AND 1165

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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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