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FDA 510(k)

CIRCAMED MONITOR REMOTE START CONDUCTANCE METER

K-Number: K874155 · 1987-11-23

ApplicantCircadian, Inc.
Decision Date1987-11-23
Product CodeKRC
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CIRCAMED MONITOR REMOTE START CONDUCTANCE METER is the device name listed in this FDA 510(k) record. The listed applicant is Circadian, Inc.. It received FDA 510(k) clearance on 1987-11-23 under 510(k) number K874155. The device is classified under product code KRC. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CIRCAMED MONITOR REMOTE START CONDUCTANCE METER?

CIRCAMED MONITOR REMOTE START CONDUCTANCE METER is a medical device that received FDA 510(k) clearance on 1987-11-23. The listed applicant is Circadian, Inc.. The 510(k) number is K874155.

When did CIRCAMED MONITOR REMOTE START CONDUCTANCE METER receive FDA 510(k) clearance?

CIRCAMED MONITOR REMOTE START CONDUCTANCE METER received FDA 510(k) clearance on 1987-11-23, under 510(k) number K874155.

Who is the listed applicant for CIRCAMED MONITOR REMOTE START CONDUCTANCE METER?

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

What is the FDA product code for CIRCAMED MONITOR REMOTE START CONDUCTANCE METER?

The FDA product code for CIRCAMED MONITOR REMOTE START CONDUCTANCE METER is KRC.

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Other records listing Circadian, 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.

K921878SCANMATE IIIK894956CIRCAMED HOLTER VERSION 4K874641CIRCADIAN STRESS TEST IIK871251CIRCAMED FULL DISCLOSURE SYSTEMK860973CIRCADIAN STRESS TEST SYSTEMK851517CIRCA MED SINGLE-CHANNEL-AMBULATORY CARDIAC MONITO

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Related Devices (Code: KRC)

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.

K023713SONOPREP IMPEDANCE DIAGNOSTICS (IDX) SYSTEM, MODEL D1000Sontra Medical, Inc.K872370BIOMA 3500E.B.S., Inc.K874327SKIN PREP ANALYZERMarquette Electronics, Inc.K840358IMPEDANCE/8200 MONITOR-MODEL 8300Aequitron Medical, Inc.K833619CONDUCTANCE METERCircadian, Inc.K830823Z VIEW METER MODEL 300Lintronics Industries, 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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