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FDA 510(k)

SYSTEM 1085 BODY PLETHYSMOGRAPH

K-Number: K852088 · 1985-07-30

ApplicantMedical Graphics Corp.
Decision Date1985-07-30
Product CodeCCM
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SYSTEM 1085 BODY 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 1985-07-30 under 510(k) number K852088. 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 SYSTEM 1085 BODY PLETHYSMOGRAPH?

SYSTEM 1085 BODY PLETHYSMOGRAPH is a medical device that received FDA 510(k) clearance on 1985-07-30. The listed applicant is Medical Graphics Corp.. The 510(k) number is K852088.

When did SYSTEM 1085 BODY PLETHYSMOGRAPH receive FDA 510(k) clearance?

SYSTEM 1085 BODY PLETHYSMOGRAPH received FDA 510(k) clearance on 1985-07-30, under 510(k) number K852088.

Who is the listed applicant for SYSTEM 1085 BODY 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 SYSTEM 1085 BODY PLETHYSMOGRAPH?

The FDA product code for SYSTEM 1085 BODY PLETHYSMOGRAPH is CCM.

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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: 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 GmbHK9432591085 ULTIMATE E PLETHYSMOGRAPHMedical Graphics Corp.K893420MASTERLAB PFT AND MASTERLAB BODY BOXQuinton, Inc.K853390INFANT BODY TESTErich Jaeger, Inc.K852102COLLIN BODY PLETHYSMOGRAPH PLUS SYSTEMWarren E. Collins, 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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