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FDA 510(k)

MICROTHERM MT-501 & MT-502

K-Number: K854007 · 1985-11-08

Decision Date1985-11-08
Product CodeFLL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MICROTHERM MT-501 & MT-502 is the device name listed in this FDA 510(k) record. The listed applicant is Medequi, Division of King Yip Co., Inc.. It received FDA 510(k) clearance on 1985-11-08 under 510(k) number K854007. The device is classified under product code FLL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICROTHERM MT-501 & MT-502?

MICROTHERM MT-501 & MT-502 is a medical device that received FDA 510(k) clearance on 1985-11-08. The listed applicant is Medequi, Division of King Yip Co., Inc.. The 510(k) number is K854007.

When did MICROTHERM MT-501 & MT-502 receive FDA 510(k) clearance?

MICROTHERM MT-501 & MT-502 received FDA 510(k) clearance on 1985-11-08, under 510(k) number K854007.

Who is the listed applicant for MICROTHERM MT-501 & MT-502?

The FDA 510(k) record lists Medequi, Division of King Yip Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MICROTHERM MT-501 & MT-502?

The FDA product code for MICROTHERM MT-501 & MT-502 is FLL.

Related Clinical Trials

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.

Other records listing Medequi, Division of King Yip Co., Inc. 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.

Related Devices (Code: FLL)

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.

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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