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FDA 510(k)

PAQ10 PAPER CHART RECORDER

K-Number: K894607 · 1989-10-26

ApplicantProtocol Systems, Inc.
Decision Date1989-10-26
Product CodeDSF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PAQ10 PAPER CHART RECORDER is the device name listed in this FDA 510(k) record. The listed applicant is Protocol Systems, Inc.. It received FDA 510(k) clearance on 1989-10-26 under 510(k) number K894607. 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 PAQ10 PAPER CHART RECORDER?

PAQ10 PAPER CHART RECORDER is a medical device that received FDA 510(k) clearance on 1989-10-26. The listed applicant is Protocol Systems, Inc.. The 510(k) number is K894607.

When did PAQ10 PAPER CHART RECORDER receive FDA 510(k) clearance?

PAQ10 PAPER CHART RECORDER received FDA 510(k) clearance on 1989-10-26, under 510(k) number K894607.

Who is the listed applicant for PAQ10 PAPER CHART RECORDER?

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

What is the FDA product code for PAQ10 PAPER CHART RECORDER?

The FDA product code for PAQ10 PAPER CHART RECORDER 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 Protocol Systems, 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.

K002725MICROPAQ, MODELS 402 AND 404K972121ACUITY CENTRAL STATIONK951246PROPAQ ENCORE 200 SERIES MONITOR WITH NEONATAL MODE AND IMPEDANCE PNEUMOGRAPHY OPTIONSK945071PROPAQ 200 MONITORK935846MODEL ACUITY CENTRAL STATIONK934711PROPAQ ECG TELEMETRY OPTION

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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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