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FDA 510(k)

SEEDNET/SEEDNETGOLD, CRYOTHERA AND CRYO-HIT SYSTEMS

K-Number: K060144 · 2006-02-13

ApplicantGalil Medical , Ltd.
Decision Date2006-02-13
Product CodeGEH
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SEEDNET/SEEDNETGOLD, CRYOTHERA AND CRYO-HIT SYSTEMS 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 2006-02-13 under 510(k) number K060144. 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/SEEDNETGOLD, CRYOTHERA AND CRYO-HIT SYSTEMS?

SEEDNET/SEEDNETGOLD, CRYOTHERA AND CRYO-HIT SYSTEMS is a medical device that received FDA 510(k) clearance on 2006-02-13. The listed applicant is Galil Medical , Ltd.. The 510(k) number is K060144.

When did SEEDNET/SEEDNETGOLD, CRYOTHERA AND CRYO-HIT SYSTEMS receive FDA 510(k) clearance?

SEEDNET/SEEDNETGOLD, CRYOTHERA AND CRYO-HIT SYSTEMS received FDA 510(k) clearance on 2006-02-13, under 510(k) number K060144.

Who is the listed applicant for SEEDNET/SEEDNETGOLD, CRYOTHERA AND CRYO-HIT SYSTEMS?

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/SEEDNETGOLD, CRYOTHERA AND CRYO-HIT SYSTEMS?

The FDA product code for SEEDNET/SEEDNETGOLD, CRYOTHERA AND CRYO-HIT SYSTEMS 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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