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FDA 510(k)

MONITOR SCOPES, MODELS 9502, 9503

K-Number: K790004 · 1979-02-28

ApplicantC-V Monitors Corp.
Decision Date1979-02-28
Product CodeDRT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MONITOR SCOPES, MODELS 9502, 9503 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 1979-02-28 under 510(k) number K790004. The device is classified under product code DRT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MONITOR SCOPES, MODELS 9502, 9503?

MONITOR SCOPES, MODELS 9502, 9503 is a medical device that received FDA 510(k) clearance on 1979-02-28. The listed applicant is C-V Monitors Corp.. The 510(k) number is K790004.

When did MONITOR SCOPES, MODELS 9502, 9503 receive FDA 510(k) clearance?

MONITOR SCOPES, MODELS 9502, 9503 received FDA 510(k) clearance on 1979-02-28, under 510(k) number K790004.

Who is the listed applicant for MONITOR SCOPES, MODELS 9502, 9503?

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 MONITOR SCOPES, MODELS 9502, 9503?

The FDA product code for MONITOR SCOPES, MODELS 9502, 9503 is DRT.

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 9529K781867WRITER, GEMINI-3K780572DCG PREAMPLIFIER MODULEK780571BLOOD PRESSURE MODULE

Related Devices (Code: DRT)

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.

K254058DistaSense(TM) (v1)Life Detection TechnologiesK261286The Circadia C300 System (C300)Circadia Health, Inc.K252676The Circadia C300 System (C300)Circadia Health, Inc.K253388Sleepiz One+ (Model 2.5)Sleepiz AGK251364Sleepiz One+ (2.5)Sleepiz AGK234003The Circadia C200 SystemCircadia Technologies, Ltd.

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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