PMT DEPTHALON DEPTH #2102— 510(k) K802152

Name: FDA 510(k) clearance K802152
Creator: U.S. Food and Drug Administration
Published: 1980-11-19

Substantially Equivalent

Progress Mankind Technology

FDA 510(k) clearance K802152 for PMT DEPTHALON DEPTH #2102, Substantially Equivalent on 1980-11-19. Applicant: Progress Mankind Technology. Device class: 2.

Clearance details

Applicant: Progress Mankind Technology
Product code: Code GZL
Device class: Class 2
Regulation: 21 CFR 882.1330
Advisory panel: Neurology
Date received: 1980-09-08
Decision date: 1980-11-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hopkins, MN, US

Download summary PDF View on FDA.gov ↗

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