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FDA 510(k)

SEEDNET, SEEDNET GOLD, CRYOHIT, CRYO THERA

K-Number: K060390 · 2006-04-27

ApplicantGalil Medical , Ltd.
Decision Date2006-04-27
Product CodeGEH
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SEEDNET, SEEDNET GOLD, CRYOHIT, CRYO THERA is the device name listed in this FDA 510(k) record. The listed applicant is Galil Medical , Ltd.. It received FDA 510(k) clearance on 2006-04-27 under 510(k) number K060390. 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 SEEDNET, SEEDNET GOLD, CRYOHIT, CRYO THERA?

SEEDNET, SEEDNET GOLD, CRYOHIT, CRYO THERA is a medical device that received FDA 510(k) clearance on 2006-04-27. The listed applicant is Galil Medical , Ltd.. The 510(k) number is K060390.

When did SEEDNET, SEEDNET GOLD, CRYOHIT, CRYO THERA receive FDA 510(k) clearance?

SEEDNET, SEEDNET GOLD, CRYOHIT, CRYO THERA received FDA 510(k) clearance on 2006-04-27, under 510(k) number K060390.

Who is the listed applicant for SEEDNET, SEEDNET GOLD, CRYOHIT, CRYO THERA?

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

What is the FDA product code for SEEDNET, SEEDNET GOLD, CRYOHIT, CRYO THERA?

The FDA product code for SEEDNET, SEEDNET GOLD, CRYOHIT, CRYO THERA is GEH.

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Related Devices (Code: GEH)

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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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