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FDA 510(k)

50MM WRITER MODEL CVM 9529

K-Number: K792099 · 1979-10-26

ApplicantC-V Monitors Corp.
Decision Date1979-10-26
Product CodeDSF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

50MM WRITER MODEL CVM 9529 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 1979-10-26 under 510(k) number K792099. The device is classified under product code DSF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 50MM WRITER MODEL CVM 9529?

50MM WRITER MODEL CVM 9529 is a medical device that received FDA 510(k) clearance on 1979-10-26. The listed applicant is C-V Monitors Corp.. The 510(k) number is K792099.

When did 50MM WRITER MODEL CVM 9529 receive FDA 510(k) clearance?

50MM WRITER MODEL CVM 9529 received FDA 510(k) clearance on 1979-10-26, under 510(k) number K792099.

Who is the listed applicant for 50MM WRITER MODEL CVM 9529?

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 50MM WRITER MODEL CVM 9529?

The FDA product code for 50MM WRITER MODEL CVM 9529 is DSF.

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.

K790004MONITOR SCOPES, MODELS 9502, 9503K781867WRITER, GEMINI-3K780572DCG PREAMPLIFIER MODULEK780571BLOOD PRESSURE MODULE

Related Devices (Code: DSF)

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.

K910871EDENTEC DIGITAL CHARTER MODEL 3710Edentec Corp.K912929DASH IVAstro-Med, Inc.K905856MODEL 556 MONITORGe Medical Systems Information TechnologiesK902586GRI LASERGRAPH(TM) ECG PAPERGri Medical Products, Inc.K902230COLORADO COLOR IMAGING RECORDERHoneywell, Inc.K901385GABRIEL MEDICAL CLS THERMAL RECORDERGabriel Medical, 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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