SATELLITE A BLOOD ACETAMINOPHEN MONITORING SYSTEM— 510(k) K897118

Substantially Equivalent

Medisense, Inc.

FDA 510(k) clearance K897118 for SATELLITE A BLOOD ACETAMINOPHEN MONITORING SYSTEM, Substantially Equivalent on 1990-05-10. Applicant: Medisense, Inc..

Clearance details

Applicant: Medisense, Inc.
Product code: Code LDP
Advisory panel: Clinical Toxicology
Date received: 1989-12-26
Decision date: 1990-05-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Cambridge, MA, US

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Adverse events under product code LDP

product code LDP

Other: 1
Total: 1

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.