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FDA 510(k)

MIDA SYSTEM, MODELS 1000/1100

K-Number: K896396 · 1990-01-18

ApplicantMedical Graphics Corp.
Decision Date1990-01-18
Product CodeDYC
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MIDA SYSTEM, MODELS 1000/1100 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 1990-01-18 under 510(k) number K896396. The device is classified under product code DYC. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MIDA SYSTEM, MODELS 1000/1100?

MIDA SYSTEM, MODELS 1000/1100 is a medical device that received FDA 510(k) clearance on 1990-01-18. The listed applicant is Medical Graphics Corp.. The 510(k) number is K896396.

When did MIDA SYSTEM, MODELS 1000/1100 receive FDA 510(k) clearance?

MIDA SYSTEM, MODELS 1000/1100 received FDA 510(k) clearance on 1990-01-18, under 510(k) number K896396.

Who is the listed applicant for MIDA SYSTEM, MODELS 1000/1100?

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 MIDA SYSTEM, MODELS 1000/1100?

The FDA product code for MIDA SYSTEM, MODELS 1000/1100 is DYC.

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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: DYC)

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.

K023414MIDA ALGORITHM REV. BOrtivus ABK823934CARIEL F12OdamK810529DIRECT WRITING VECTORCARDIOGRAPHElmed, 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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