FDA 510(k)

DINAMAP MODEL 846

K-Number: K781053 · 1978-09-07

Decision Date1978-09-07

Product CodeDSK

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

DINAMAP MODEL 846 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 1978-09-07 under 510(k) number K781053. The device is classified under product code DSK. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DINAMAP MODEL 846?

DINAMAP MODEL 846 is a medical device that received FDA 510(k) clearance on 1978-09-07. The listed applicant is Applied Medical Research. The 510(k) number is K781053.

When did DINAMAP MODEL 846 receive FDA 510(k) clearance?

DINAMAP MODEL 846 received FDA 510(k) clearance on 1978-09-07, under 510(k) number K781053.

Who is the listed applicant for DINAMAP MODEL 846?

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 DINAMAP MODEL 846?

The FDA product code for DINAMAP MODEL 846 is DSK.

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Other records listing Applied Medical Research as applicant

K800025DINAMAP RESEARCH MONITOR 1245 K791580CEREBRAL FUNCTION MONITOR 870 K791159DINAMAP MODEL 855 K790322OPTIONAL ACCESSORY FOOT SWITCH MODEL 100 K790328MODEL 1051, MONITOR K782073DINAMAP MODELS 1160 AND 1165

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Related Devices (Code: DSK)

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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.