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FDA 510(k)

CPE 2000 CARDIO PULMONARY ERGOMETER

K-Number: K874925 · 1988-01-19

ApplicantMedical Graphics Corp.
Decision Date1988-01-19
Product CodeKRI
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CPE 2000 CARDIO PULMONARY ERGOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Medical Graphics Corp.. It received FDA 510(k) clearance on 1988-01-19 under 510(k) number K874925. The device is classified under product code KRI. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CPE 2000 CARDIO PULMONARY ERGOMETER?

CPE 2000 CARDIO PULMONARY ERGOMETER is a medical device that received FDA 510(k) clearance on 1988-01-19. The listed applicant is Medical Graphics Corp.. The 510(k) number is K874925.

When did CPE 2000 CARDIO PULMONARY ERGOMETER receive FDA 510(k) clearance?

CPE 2000 CARDIO PULMONARY ERGOMETER received FDA 510(k) clearance on 1988-01-19, under 510(k) number K874925.

Who is the listed applicant for CPE 2000 CARDIO PULMONARY ERGOMETER?

The FDA 510(k) record lists Medical Graphics Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CPE 2000 CARDIO PULMONARY ERGOMETER?

The FDA product code for CPE 2000 CARDIO PULMONARY ERGOMETER is KRI.

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Other records listing Medical Graphics 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.

K152585Resmon PRO FULLK070858EXPRESS SERIESK061731MEDGRAPHICS ULTIMA SYSTEMK955432CPX, CCM, CATH WITH 15% CO2K9432591085 ULTIMATE E PLETHYSMOGRAPHK923209MEDGRAPHICS EXERCISE CONSULT

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Related Devices (Code: KRI)

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.

K0203653TM MYOCARDIAL NEEDLE-TEMPERATURE PROBE3t Medical Systems, LLCK992635INTERFACE MODULE IDDDStoeckert InstrumenteK990512STOCKERT POWER SUPPLY UNIT FOR S3 COMPONENTSStoeckert InstrumenteK934782AMMEX TUBING ORGANIZERAmmex Cardiopulmonary Corp.K926233CARDIO2 CYCLEErgometrix, Inc.K922404TUBE GRIPGeorgia Medical Products, 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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