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FDA 510(k)

MC II (TM), MODEL 7200S

K-Number: K903161 · 1991-03-27

ApplicantMedical Devices, Inc.
Decision Date1991-03-27
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MC II (TM), MODEL 7200S is the device name listed in this FDA 510(k) record. The listed applicant is Medical Devices, Inc.. It received FDA 510(k) clearance on 1991-03-27 under 510(k) number K903161. The device is classified under product code GZJ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MC II (TM), MODEL 7200S?

MC II (TM), MODEL 7200S is a medical device that received FDA 510(k) clearance on 1991-03-27. The listed applicant is Medical Devices, Inc.. The 510(k) number is K903161.

When did MC II (TM), MODEL 7200S receive FDA 510(k) clearance?

MC II (TM), MODEL 7200S received FDA 510(k) clearance on 1991-03-27, under 510(k) number K903161.

Who is the listed applicant for MC II (TM), MODEL 7200S?

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

What is the FDA product code for MC II (TM), MODEL 7200S?

The FDA product code for MC II (TM), MODEL 7200S is GZJ.

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Other records listing Medical Devices, Inc. as applicant

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Related Devices (Code: GZJ)

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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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