Decision Date1985-11-15
Product CodeFTC
Advisory CommitteeSU
DecisionSubstantially Equivalent
Device Summary
G-T 1000 is the device name listed in this FDA 510(k) record. The listed applicant is G-T Products. It received FDA 510(k) clearance on 1985-11-15 under 510(k) number K854020. The device is classified under product code FTC. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the G-T 1000?
G-T 1000 is a medical device that received FDA 510(k) clearance on 1985-11-15. The listed applicant is G-T Products. The 510(k) number is K854020.
When did G-T 1000 receive FDA 510(k) clearance?
G-T 1000 received FDA 510(k) clearance on 1985-11-15, under 510(k) number K854020.
Who is the listed applicant for G-T 1000?
The FDA 510(k) record lists G-T Products as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for G-T 1000?
The FDA product code for G-T 1000 is FTC.
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Official Source
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