MODELS 134, 135 & 136 TRANSFER CART/TABLE— 510(k) K844711

Name: FDA 510(k) clearance K844711
Creator: U.S. Food and Drug Administration
Published: 1985-03-05

Substantially Equivalent

Tri W-G, Inc.

FDA 510(k) clearance K844711 for MODELS 134, 135 & 136 TRANSFER CART/TABLE, Substantially Equivalent on 1985-03-05. Applicant: Tri W-G, Inc.. Device class: 2.

Clearance details

Applicant: Tri W-G, Inc.
Product code: Code INK
Device class: Class 2
Regulation: 21 CFR 890.3690
Advisory panel: Physical Medicine
Date received: 1984-12-03
Decision date: 1985-03-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Valley City, ND, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code INK

product code INK

Malfunction: 708
Other: 1
Total: 709

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.