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FDA 510(k)

MEDGRAPHICS EXERCISE CONSULT

K-Number: K923209 · 1993-03-11

ApplicantMedical Graphics Corp.
Decision Date1993-03-11
Product CodeBZM
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MEDGRAPHICS EXERCISE CONSULT 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 1993-03-11 under 510(k) number K923209. The device is classified under product code BZM. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDGRAPHICS EXERCISE CONSULT?

MEDGRAPHICS EXERCISE CONSULT is a medical device that received FDA 510(k) clearance on 1993-03-11. The listed applicant is Medical Graphics Corp.. The 510(k) number is K923209.

When did MEDGRAPHICS EXERCISE CONSULT receive FDA 510(k) clearance?

MEDGRAPHICS EXERCISE CONSULT received FDA 510(k) clearance on 1993-03-11, under 510(k) number K923209.

Who is the listed applicant for MEDGRAPHICS EXERCISE CONSULT?

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 MEDGRAPHICS EXERCISE CONSULT?

The FDA product code for MEDGRAPHICS EXERCISE CONSULT is BZM.

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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 PLETHYSMOGRAPHK912906MEDGRAPHICS PF/DX

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Related Devices (Code: BZM)

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.

K102229PULMOTRACK 2020 SYSTEMKarmelsonixK090863PERSONAL WHEEZOMETERKarmelsonixK071955WIM-PC, MODEL 1010KarmelsonixK012387STG MULTICHANNEL LUNG SOUND ANALYSIS SYSTEMStethographics, Inc.K980878PULMOTRACK,MODEL 1010Karmel Medical Acoustic Technologies , Ltd.K974200ORCA CARDIOPULMONARY EXERCISE TESTING SYSTEMOrca Diagnostics 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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