PATIENT CABLE— 510(k) K932704

Name: FDA 510(k) clearance K932704
Creator: U.S. Food and Drug Administration
Published: 1993-12-27

Substantially Equivalent

Sentry Medical Products, Inc.

FDA 510(k) clearance K932704 for PATIENT CABLE, Substantially Equivalent on 1993-12-27. Applicant: Sentry Medical Products, Inc.. Device class: 2.

Clearance details

Applicant: Sentry Medical Products, Inc.
Product code: Product code DSA
Device class: Class 2
Regulation: 21 CFR 870.2900
Advisory panel: Cardiovascular
Date received: 1993-06-03
Decision date: 1993-12-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Irvine, CA, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code DSA

product code DSA

Death: 2
Total: 2

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.