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FDA 510(k)

GO-BETWEEN

K-Number: K803129 · 1981-01-08

ApplicantAgri Hort
Decision Date1981-01-08
Product CodeJES
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

GO-BETWEEN is the device name listed in this FDA 510(k) record. The listed applicant is Agri Hort. It received FDA 510(k) clearance on 1981-01-08 under 510(k) number K803129. The device is classified under product code JES. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GO-BETWEEN?

GO-BETWEEN is a medical device that received FDA 510(k) clearance on 1981-01-08. The listed applicant is Agri Hort. The 510(k) number is K803129.

When did GO-BETWEEN receive FDA 510(k) clearance?

GO-BETWEEN received FDA 510(k) clearance on 1981-01-08, under 510(k) number K803129.

Who is the listed applicant for GO-BETWEEN?

The FDA 510(k) record lists Agri Hort as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GO-BETWEEN?

The FDA product code for GO-BETWEEN is JES.

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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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