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FDA 510(k)

MT-700 MT-750 FT-350

K-Number: K842704 · 1984-08-01

ApplicantCryomedics, Inc.
Decision Date1984-08-01
Product CodeGEH
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MT-700 MT-750 FT-350 is the device name listed in this FDA 510(k) record. The listed applicant is Cryomedics, Inc.. It received FDA 510(k) clearance on 1984-08-01 under 510(k) number K842704. The device is classified under product code GEH. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MT-700 MT-750 FT-350?

MT-700 MT-750 FT-350 is a medical device that received FDA 510(k) clearance on 1984-08-01. The listed applicant is Cryomedics, Inc.. The 510(k) number is K842704.

When did MT-700 MT-750 FT-350 receive FDA 510(k) clearance?

MT-700 MT-750 FT-350 received FDA 510(k) clearance on 1984-08-01, under 510(k) number K842704.

Who is the listed applicant for MT-700 MT-750 FT-350?

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

What is the FDA product code for MT-700 MT-750 FT-350?

The FDA product code for MT-700 MT-750 FT-350 is GEH.

Other records listing Cryomedics, Inc. as applicant

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Related Devices (Code: GEH)

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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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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