FDA 510(k)

T-M (TIME-MOTION) OPTION

K-Number: K761139 · 1976-12-16

Decision Date1976-12-16

Product CodeHGM

Advisory CommitteeOB

DecisionSubstantially Equivalent

Device Summary

T-M (TIME-MOTION) OPTION is the device name listed in this FDA 510(k) record. The listed applicant is G.D. Searle and Co.. It received FDA 510(k) clearance on 1976-12-16 under 510(k) number K761139. The device is classified under product code HGM. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the T-M (TIME-MOTION) OPTION?

T-M (TIME-MOTION) OPTION is a medical device that received FDA 510(k) clearance on 1976-12-16. The listed applicant is G.D. Searle and Co.. The 510(k) number is K761139.

When did T-M (TIME-MOTION) OPTION receive FDA 510(k) clearance?

T-M (TIME-MOTION) OPTION received FDA 510(k) clearance on 1976-12-16, under 510(k) number K761139.

Who is the listed applicant for T-M (TIME-MOTION) OPTION?

The FDA 510(k) record lists G.D. Searle and Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for T-M (TIME-MOTION) OPTION?

The FDA product code for T-M (TIME-MOTION) OPTION is HGM.

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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.