THERMOMETER, DIGITAL FEVER (MEDITEMP)— 510(k) K760118

Substantially Equivalent

Johnson & Johnson Professionals, Inc.

FDA 510(k) clearance K760118 for THERMOMETER, DIGITAL FEVER (MEDITEMP), Substantially Equivalent on 1976-07-20. Applicant: Johnson & Johnson Professionals, Inc..

Clearance details

Applicant: Johnson & Johnson Professionals, Inc.
Product code: Code FLL
Advisory panel: General Hospital
Date received: 1976-06-25
Decision date: 1976-07-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Raynham, MA, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code FLL

product code FLL

Death: 3
Malfunction: 557
Total: 560

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.