TRANSPAC(R) II, DISPOSABLE TRANSDUCER— 510(k) K884823

Name: FDA 510(k) clearance K884823
Creator: U.S. Food and Drug Administration
Published: 1990-07-03

Substantially Equivalent

Abbott Laboratories

FDA 510(k) clearance K884823 for TRANSPAC(R) II, DISPOSABLE TRANSDUCER, Substantially Equivalent on 1990-07-03. Applicant: Abbott Laboratories. Device class: 2.

Clearance details

Applicant: Abbott Laboratories
Product code: Code GWM
Device class: Class 2
Regulation: 21 CFR 882.1620
Advisory panel: Neurology
Date received: 1988-11-18
Decision date: 1990-07-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Abbott Park, IL, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code GWM

product code GWM

Death: 21
Injury: 732
Malfunction: 2,063
Other: 1
Total: 2,817

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.