G5 APPARATUS T, K1, K3 & THE PRESIDENT MODEL'S— 510(k) K850851

Name: FDA 510(k) clearance K850851
Creator: U.S. Food and Drug Administration
Published: 1985-06-25

Substantially Equivalent

Physio Technology, Inc.

FDA 510(k) clearance K850851 for G5 APPARATUS T, K1, K3 & THE PRESIDENT MODEL'S, Substantially Equivalent on 1985-06-25. Applicant: Physio Technology, Inc.. Device class: 1.

Clearance details

Applicant: Physio Technology, Inc.
Product code: Code ISA
Device class: Class 1
Regulation: 21 CFR 890.5660
Advisory panel: Physical Medicine
Date received: 1985-03-01
Decision date: 1985-06-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Topeka, KS, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code ISA

product code ISA

Death: 3
Other: 1
Total: 4

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.