FDA 510(k)

PMT DEPTHALON DEPTH CORTICOGRAPHY ELEC

K-Number: K802151 · 1980-11-19

Decision Date1980-11-19

Product CodeGZL

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

PMT DEPTHALON DEPTH CORTICOGRAPHY ELEC is the device name listed in this FDA 510(k) record. The listed applicant is Progress Mankind Technology. It received FDA 510(k) clearance on 1980-11-19 under 510(k) number K802151. The device is classified under product code GZL. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PMT DEPTHALON DEPTH CORTICOGRAPHY ELEC?

PMT DEPTHALON DEPTH CORTICOGRAPHY ELEC is a medical device that received FDA 510(k) clearance on 1980-11-19. The listed applicant is Progress Mankind Technology. The 510(k) number is K802151.

When did PMT DEPTHALON DEPTH CORTICOGRAPHY ELEC receive FDA 510(k) clearance?

PMT DEPTHALON DEPTH CORTICOGRAPHY ELEC received FDA 510(k) clearance on 1980-11-19, under 510(k) number K802151.

Who is the listed applicant for PMT DEPTHALON DEPTH CORTICOGRAPHY ELEC?

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

What is the FDA product code for PMT DEPTHALON DEPTH CORTICOGRAPHY ELEC?

The FDA product code for PMT DEPTHALON DEPTH CORTICOGRAPHY ELEC is GZL.

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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.