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FDA 510(k)

RECORDER, STRIP CHART WITH PRINTER

K-Number: K781873 · 1979-01-05

ApplicantMidwest Analog & Digital, Inc.
Decision Date1979-01-05
Product CodeDSF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

RECORDER, STRIP CHART WITH PRINTER is the device name listed in this FDA 510(k) record. The listed applicant is Midwest Analog & Digital, Inc.. It received FDA 510(k) clearance on 1979-01-05 under 510(k) number K781873. 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 RECORDER, STRIP CHART WITH PRINTER?

RECORDER, STRIP CHART WITH PRINTER is a medical device that received FDA 510(k) clearance on 1979-01-05. The listed applicant is Midwest Analog & Digital, Inc.. The 510(k) number is K781873.

When did RECORDER, STRIP CHART WITH PRINTER receive FDA 510(k) clearance?

RECORDER, STRIP CHART WITH PRINTER received FDA 510(k) clearance on 1979-01-05, under 510(k) number K781873.

Who is the listed applicant for RECORDER, STRIP CHART WITH PRINTER?

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

What is the FDA product code for RECORDER, STRIP CHART WITH PRINTER?

The FDA product code for RECORDER, STRIP CHART WITH PRINTER 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 Midwest Analog & Digital, 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.

K850619BEDSIDE PATIENT MONITOR W/MODULESK780432ARRHYTHMIA PROGRAM 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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