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FDA 510(k)

SYPHGMOLOG

K-Number: K811079 · 1981-06-12

ApplicantCardiodyne General, Inc.
Decision Date1981-06-12
Product CodeDSK
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SYPHGMOLOG is the device name listed in this FDA 510(k) record. The listed applicant is Cardiodyne General, Inc.. It received FDA 510(k) clearance on 1981-06-12 under 510(k) number K811079. 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 SYPHGMOLOG?

SYPHGMOLOG is a medical device that received FDA 510(k) clearance on 1981-06-12. The listed applicant is Cardiodyne General, Inc.. The 510(k) number is K811079.

When did SYPHGMOLOG receive FDA 510(k) clearance?

SYPHGMOLOG received FDA 510(k) clearance on 1981-06-12, under 510(k) number K811079.

Who is the listed applicant for SYPHGMOLOG?

The FDA 510(k) record lists Cardiodyne General, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SYPHGMOLOG?

The FDA product code for SYPHGMOLOG 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 Cardiodyne General, Inc. 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.

K830184SPHYGMOLOG II MODEL D

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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