Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

MINIMAP MODEL 810

K-Number: K771981 · 1978-01-24

ApplicantApplied Medical Research
Decision Date1978-01-24
Product CodeDSK
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MINIMAP MODEL 810 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 1978-01-24 under 510(k) number K771981. 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 MINIMAP MODEL 810?

MINIMAP MODEL 810 is a medical device that received FDA 510(k) clearance on 1978-01-24. The listed applicant is Applied Medical Research. The 510(k) number is K771981.

When did MINIMAP MODEL 810 receive FDA 510(k) clearance?

MINIMAP MODEL 810 received FDA 510(k) clearance on 1978-01-24, under 510(k) number K771981.

Who is the listed applicant for MINIMAP MODEL 810?

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 MINIMAP MODEL 810?

The FDA product code for MINIMAP MODEL 810 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_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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

View all 22 devices →

Related Devices (Code: DSK)

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.

K231586Endophys Blood Pressure Monitor model BPM-30Endophys Technologies, LLCK160945Endophys Blood Pressure MonitorEndophys Holdings, LLCK080670MODIFICATION TO SPHYGMOCOR CARDIOVASCULAR MANAGEMENT SYSTEMAtcor MedicalK070795SPHYGMOCOR CARDIOVASCULAR MANAGEMENT SYSTEMAtcor Medical Pty, Ltd.K033738MONITORING SYSTEM, MODEL ARGUS PB-2200Schiller AGK021517ABP 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.

↑