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FDA 510(k)

1085 ULTIMATE E PLETHYSMOGRAPH

K-Number: K943259 · 1995-04-10

ApplicantMedical Graphics Corp.
Decision Date1995-04-10
Product CodeCCM
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

1085 ULTIMATE E PLETHYSMOGRAPH 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 1995-04-10 under 510(k) number K943259. The device is classified under product code CCM. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 1085 ULTIMATE E PLETHYSMOGRAPH?

1085 ULTIMATE E PLETHYSMOGRAPH is a medical device that received FDA 510(k) clearance on 1995-04-10. The listed applicant is Medical Graphics Corp.. The 510(k) number is K943259.

When did 1085 ULTIMATE E PLETHYSMOGRAPH receive FDA 510(k) clearance?

1085 ULTIMATE E PLETHYSMOGRAPH received FDA 510(k) clearance on 1995-04-10, under 510(k) number K943259.

Who is the listed applicant for 1085 ULTIMATE E PLETHYSMOGRAPH?

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 1085 ULTIMATE E PLETHYSMOGRAPH?

The FDA product code for 1085 ULTIMATE E PLETHYSMOGRAPH is CCM.

Related Clinical Trials

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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% CO2K923209MEDGRAPHICS EXERCISE CONSULTK912906MEDGRAPHICS PF/DX

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Related Devices (Code: CCM)

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.

K081823MASTERSCREEN PAED - BABY BODYViasys Healthcare GmbHK023796MS PAED-BABY BODYErich Jaeger GmbHK893420MASTERLAB PFT AND MASTERLAB BODY BOXQuinton, Inc.K853390INFANT BODY TESTErich Jaeger, Inc.K852102COLLIN BODY PLETHYSMOGRAPH PLUS SYSTEMWarren E. Collins, Inc.K852088SYSTEM 1085 BODY PLETHYSMOGRAPHMedical Graphics Corp.

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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