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FDA 510(k)

MID-CANADA MEDICAL

K-Number: K922839 · 1993-07-02

ApplicantMid-Canada Medical
Decision Date1993-07-02
Product CodeIMI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MID-CANADA MEDICAL is the device name listed in this FDA 510(k) record. The listed applicant is Mid-Canada Medical. It received FDA 510(k) clearance on 1993-07-02 under 510(k) number K922839. The device is classified under product code IMI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MID-CANADA MEDICAL?

MID-CANADA MEDICAL is a medical device that received FDA 510(k) clearance on 1993-07-02. The listed applicant is Mid-Canada Medical. The 510(k) number is K922839.

When did MID-CANADA MEDICAL receive FDA 510(k) clearance?

MID-CANADA MEDICAL received FDA 510(k) clearance on 1993-07-02, under 510(k) number K922839.

Who is the listed applicant for MID-CANADA MEDICAL?

The FDA 510(k) record lists Mid-Canada Medical as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MID-CANADA MEDICAL?

The FDA product code for MID-CANADA MEDICAL is IMI.

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Other records listing Mid-Canada Medical 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.

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Related Devices (Code: IMI)

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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