FDA 510(k)

PHO. TRAX MODEL 4000 WHOLE BODY SCAN.

K-Number: K760808 · 1976-11-05

Decision Date1976-11-05

Product CodeJAK

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

PHO. TRAX MODEL 4000 WHOLE BODY SCAN. 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 1976-11-05 under 510(k) number K760808. The device is classified under product code JAK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PHO. TRAX MODEL 4000 WHOLE BODY SCAN.?

PHO. TRAX MODEL 4000 WHOLE BODY SCAN. is a medical device that received FDA 510(k) clearance on 1976-11-05. The listed applicant is G.D. Searle and Co.. The 510(k) number is K760808.

When did PHO. TRAX MODEL 4000 WHOLE BODY SCAN. receive FDA 510(k) clearance?

PHO. TRAX MODEL 4000 WHOLE BODY SCAN. received FDA 510(k) clearance on 1976-11-05, under 510(k) number K760808.

Who is the listed applicant for PHO. TRAX MODEL 4000 WHOLE BODY SCAN.?

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 PHO. TRAX MODEL 4000 WHOLE BODY SCAN.?

The FDA product code for PHO. TRAX MODEL 4000 WHOLE BODY SCAN. is JAK.

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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.