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FDA 510(k)

SEEDNET, MODEL FP6T5, FP5T5, FP5T3

K-Number: K011950 · 2002-01-29

ApplicantGalil Medical , Ltd.
Decision Date2002-01-29
Product CodeGEH
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SEEDNET, MODEL FP6T5, FP5T5, FP5T3 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 2002-01-29 under 510(k) number K011950. 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, MODEL FP6T5, FP5T5, FP5T3?

SEEDNET, MODEL FP6T5, FP5T5, FP5T3 is a medical device that received FDA 510(k) clearance on 2002-01-29. The listed applicant is Galil Medical , Ltd.. The 510(k) number is K011950.

When did SEEDNET, MODEL FP6T5, FP5T5, FP5T3 receive FDA 510(k) clearance?

SEEDNET, MODEL FP6T5, FP5T5, FP5T3 received FDA 510(k) clearance on 2002-01-29, under 510(k) number K011950.

Who is the listed applicant for SEEDNET, MODEL FP6T5, FP5T5, FP5T3?

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, MODEL FP6T5, FP5T5, FP5T3?

The FDA product code for SEEDNET, MODEL FP6T5, FP5T5, FP5T3 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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