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FDA 510(k)

DCG PREAMPLIFIER MODULE

K-Number: K780572 · 1978-05-09

ApplicantC-V Monitors Corp.
Decision Date1978-05-09
Product CodeDRR
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DCG PREAMPLIFIER MODULE is the device name listed in this FDA 510(k) record. The listed applicant is C-V Monitors Corp.. It received FDA 510(k) clearance on 1978-05-09 under 510(k) number K780572. The device is classified under product code DRR. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DCG PREAMPLIFIER MODULE?

DCG PREAMPLIFIER MODULE is a medical device that received FDA 510(k) clearance on 1978-05-09. The listed applicant is C-V Monitors Corp.. The 510(k) number is K780572.

When did DCG PREAMPLIFIER MODULE receive FDA 510(k) clearance?

DCG PREAMPLIFIER MODULE received FDA 510(k) clearance on 1978-05-09, under 510(k) number K780572.

Who is the listed applicant for DCG PREAMPLIFIER MODULE?

The FDA 510(k) record lists C-V Monitors Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DCG PREAMPLIFIER MODULE?

The FDA product code for DCG PREAMPLIFIER MODULE is DRR.

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 C-V Monitors Corp. 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.

K79209950MM WRITER MODEL CVM 9529K790004MONITOR SCOPES, MODELS 9502, 9503K781867WRITER, GEMINI-3K780571BLOOD PRESSURE MODULE

Related Devices (Code: DRR)

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.

K022660BIOCHECK MYOGLOBIN ELISA, MODEL BC-1117Biocheck, Inc.K971570EPXPRESS SYSTEM (TIMBERWOLF REVISION) /000391Quinton Electrophysiology Corp.K925346EP AMP, MODEL #901Quinton Electrophysiology Corp.K914381HORIZON 9000/HIS OPTION AMPLIFIERMennen Medical, Inc.K911935CARDIAC ELECTROPHYSICAL LEAD SELECTOR, MODIFIEDGould, Inc.K910307CARDIOLAB AMPLIFIER MODULE (CAM)Prucka Engineering, 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.

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