MULTIMODE(TM) POWER MODULE SYSTEM— 510(k) K881463

Name: FDA 510(k) clearance K881463
Creator: U.S. Food and Drug Administration
Published: 1988-07-18

Substantially Equivalent

Dufco Electronics, Inc.

FDA 510(k) clearance K881463 for MULTIMODE(TM) POWER MODULE SYSTEM, Substantially Equivalent on 1988-07-18. Applicant: Dufco Electronics, Inc.. Device class: 2.

Clearance details

Applicant: Dufco Electronics, Inc.
Product code: Code ITI
Device class: Class 2
Regulation: 21 CFR 890.3860
Advisory panel: Physical Medicine
Date received: 1988-04-07
Decision date: 1988-07-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Cambria, CA, US

Download summary PDF View on FDA.gov ↗

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More clearances from Dufco Electronics, Inc.

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K881461 — MULTIMODE(TM) INTERFACE SYSTEM FOR MEYRA WHEELCH.1988-07-18
K881462 — UNIMODE(TM) POWER MODULE SYSTEM1988-07-18
K881464 — MULTIMODE(TM) INTERFACE SYS. FOR EVEREST & JENNING1988-07-18

Adverse events under product code ITI

product code ITI

Death: 34
Injury: 778
Malfunction: 1,085
Other: 1
Total: 1,898

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.