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FDA 510(k)

MDT/HARVEY MODEL 7000 & 8000 CHEMICLAVE

K-Number: K924380 · 1994-02-16

ApplicantMdt Corp., Inc.
Decision Date1994-02-16
Product CodeMLR
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MDT/HARVEY MODEL 7000 & 8000 CHEMICLAVE 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 1994-02-16 under 510(k) number K924380. The device is classified under product code MLR. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MDT/HARVEY MODEL 7000 & 8000 CHEMICLAVE?

MDT/HARVEY MODEL 7000 & 8000 CHEMICLAVE is a medical device that received FDA 510(k) clearance on 1994-02-16. The listed applicant is Mdt Corp., Inc.. The 510(k) number is K924380.

When did MDT/HARVEY MODEL 7000 & 8000 CHEMICLAVE receive FDA 510(k) clearance?

MDT/HARVEY MODEL 7000 & 8000 CHEMICLAVE received FDA 510(k) clearance on 1994-02-16, under 510(k) number K924380.

Who is the listed applicant for MDT/HARVEY MODEL 7000 & 8000 CHEMICLAVE?

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 MODEL 7000 & 8000 CHEMICLAVE?

The FDA product code for MDT/HARVEY MODEL 7000 & 8000 CHEMICLAVE is MLR.

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Other records listing Mdt Corp., Inc. as applicant

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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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