FDA 510(k)

DINAMAP MODELS 1160 AND 1165

K-Number: K782073 · 1979-02-23

Decision Date1979-02-23

Product CodeDSK

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

DINAMAP MODELS 1160 AND 1165 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 1979-02-23 under 510(k) number K782073. 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 MODELS 1160 AND 1165?

DINAMAP MODELS 1160 AND 1165 is a medical device that received FDA 510(k) clearance on 1979-02-23. The listed applicant is Applied Medical Research. The 510(k) number is K782073.

When did DINAMAP MODELS 1160 AND 1165 receive FDA 510(k) clearance?

DINAMAP MODELS 1160 AND 1165 received FDA 510(k) clearance on 1979-02-23, under 510(k) number K782073.

Who is the listed applicant for DINAMAP MODELS 1160 AND 1165?

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 MODELS 1160 AND 1165?

The FDA product code for DINAMAP MODELS 1160 AND 1165 is DSK.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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 K781053DINAMAP MODEL 846

View all 22 devices →

Related Devices (Code: DSK)

K231586Endophys Blood Pressure Monitor model BPM-30Endophys Technologies, LLC K160945Endophys Blood Pressure MonitorEndophys Holdings, LLC K080670MODIFICATION TO SPHYGMOCOR CARDIOVASCULAR MANAGEMENT SYSTEMAtcor Medical K070795SPHYGMOCOR CARDIOVASCULAR MANAGEMENT SYSTEMAtcor Medical Pty, Ltd.K033738MONITORING SYSTEM, MODEL ARGUS PB-2200Schiller AG K021517ABP FOR WINDOWSRozinn Electronics, Inc.

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.