Patient Monitoring System
FDA 510(k) K760559 · General Electric Co.
510(k) numberK760559
Submission
- Device name
- Patient Monitoring System
- Applicant
- General Electric Co.
Mchenry, IL, US - Received
- September 2, 1976
- Decision date
- September 10, 1976
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
No product code recorded.
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Questions and answers
When was Patient Monitoring System cleared by the FDA?
Patient Monitoring System (K760559) received a 510(k) decision of Substantially Equivalent on September 10, 1976, 8 days after the submission was received.