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FDA 510(k)

CRYOMEDICAL INSTRUMENTS CRYO-PAC SYSTEMS

K-Number: K050272 · 2005-03-24

ApplicantCryomedical Instruments, Ltd.
Decision Date2005-03-24
Product CodeGXH
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

CRYOMEDICAL INSTRUMENTS CRYO-PAC SYSTEMS is the device name listed in this FDA 510(k) record. The listed applicant is Cryomedical Instruments, Ltd.. It received FDA 510(k) clearance on 2005-03-24 under 510(k) number K050272. The device is classified under product code GXH. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CRYOMEDICAL INSTRUMENTS CRYO-PAC SYSTEMS?

CRYOMEDICAL INSTRUMENTS CRYO-PAC SYSTEMS is a medical device that received FDA 510(k) clearance on 2005-03-24. The listed applicant is Cryomedical Instruments, Ltd.. The 510(k) number is K050272.

When did CRYOMEDICAL INSTRUMENTS CRYO-PAC SYSTEMS receive FDA 510(k) clearance?

CRYOMEDICAL INSTRUMENTS CRYO-PAC SYSTEMS received FDA 510(k) clearance on 2005-03-24, under 510(k) number K050272.

Who is the listed applicant for CRYOMEDICAL INSTRUMENTS CRYO-PAC SYSTEMS?

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

What is the FDA product code for CRYOMEDICAL INSTRUMENTS CRYO-PAC SYSTEMS?

The FDA product code for CRYOMEDICAL INSTRUMENTS CRYO-PAC SYSTEMS is GXH.

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Related Devices (Code: GXH)

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

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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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