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FDA 510(k)

CENTURION CHART RECORDER

K-Number: K822432 · 1982-11-01

ApplicantClinical Data, Inc.
Decision Date1982-11-01
Product CodeDSF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CENTURION CHART RECORDER is the device name listed in this FDA 510(k) record. The listed applicant is Clinical Data, Inc.. It received FDA 510(k) clearance on 1982-11-01 under 510(k) number K822432. 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 CENTURION CHART RECORDER?

CENTURION CHART RECORDER is a medical device that received FDA 510(k) clearance on 1982-11-01. The listed applicant is Clinical Data, Inc.. The 510(k) number is K822432.

When did CENTURION CHART RECORDER receive FDA 510(k) clearance?

CENTURION CHART RECORDER received FDA 510(k) clearance on 1982-11-01, under 510(k) number K822432.

Who is the listed applicant for CENTURION CHART RECORDER?

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

What is the FDA product code for CENTURION CHART RECORDER?

The FDA product code for CENTURION CHART RECORDER is DSF.

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Related Devices (Code: DSF)

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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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