PATIENT MONITOR #404— 510(k) K831319
Substantially EquivalentAnalogic Corp.
FDA 510(k) clearance K831319 for PATIENT MONITOR #404, Substantially Equivalent on 1984-03-22. Applicant: Analogic Corp.. Device class: 2.
Clearance details
- Applicant
- Analogic Corp.
- Product code
- Code KLK
- Device class
- Class 2
- Regulation
- 21 CFR 868.2500
- Advisory panel
- Anesthesiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Walker, MI, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.