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FDA 510(k)

WRITER, GEMINI-3

K-Number: K781867 · 1979-01-05

ApplicantC-V Monitors Corp.
Decision Date1979-01-05
Product CodeDSF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

WRITER, GEMINI-3 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 1979-01-05 under 510(k) number K781867. 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 WRITER, GEMINI-3?

WRITER, GEMINI-3 is a medical device that received FDA 510(k) clearance on 1979-01-05. The listed applicant is C-V Monitors Corp.. The 510(k) number is K781867.

When did WRITER, GEMINI-3 receive FDA 510(k) clearance?

WRITER, GEMINI-3 received FDA 510(k) clearance on 1979-01-05, under 510(k) number K781867.

Who is the listed applicant for WRITER, GEMINI-3?

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 WRITER, GEMINI-3?

The FDA product code for WRITER, GEMINI-3 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.

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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, 9503K780572DCG 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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