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FDA 510(k)

MDT/HARVEY MC-8 AND MC-10

K-Number: K924955 · 1993-10-15

ApplicantMdt Corp., Inc.
Decision Date1993-10-15
Product CodeFLE
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MDT/HARVEY MC-8 AND MC-10 is the device name listed in this FDA 510(k) record. The listed applicant is Mdt Corp., Inc.. It received FDA 510(k) clearance on 1993-10-15 under 510(k) number K924955. The device is classified under product code FLE. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MDT/HARVEY MC-8 AND MC-10?

MDT/HARVEY MC-8 AND MC-10 is a medical device that received FDA 510(k) clearance on 1993-10-15. The listed applicant is Mdt Corp., Inc.. The 510(k) number is K924955.

When did MDT/HARVEY MC-8 AND MC-10 receive FDA 510(k) clearance?

MDT/HARVEY MC-8 AND MC-10 received FDA 510(k) clearance on 1993-10-15, under 510(k) number K924955.

Who is the listed applicant for MDT/HARVEY MC-8 AND MC-10?

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

What is the FDA product code for MDT/HARVEY MC-8 AND MC-10?

The FDA product code for MDT/HARVEY MC-8 AND MC-10 is FLE.

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Other records listing Mdt Corp., Inc. as applicant

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Related Devices (Code: FLE)

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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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