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FDA 510(k)

SEEDNET, SEEDNET GOLD, CRYOHIT, CRYOTHERA

K-Number: K052530 · 2005-11-18

ApplicantGalil Medical , Ltd.
Decision Date2005-11-18
Product CodeGEH
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SEEDNET, SEEDNET GOLD, CRYOHIT, CRYOTHERA 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 2005-11-18 under 510(k) number K052530. 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, CRYOTHERA?

SEEDNET, SEEDNET GOLD, CRYOHIT, CRYOTHERA is a medical device that received FDA 510(k) clearance on 2005-11-18. The listed applicant is Galil Medical , Ltd.. The 510(k) number is K052530.

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

SEEDNET, SEEDNET GOLD, CRYOHIT, CRYOTHERA received FDA 510(k) clearance on 2005-11-18, under 510(k) number K052530.

Who is the listed applicant for SEEDNET, SEEDNET GOLD, CRYOHIT, CRYOTHERA?

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, CRYOTHERA?

The FDA product code for SEEDNET, SEEDNET GOLD, CRYOHIT, CRYOTHERA is 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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