MODEL 78850 OXYGEN MONITOR— 510(k) K812167
Substantially EquivalentHewlett-Packard Co.
FDA 510(k) clearance K812167 for MODEL 78850 OXYGEN MONITOR, Substantially Equivalent on 1981-08-31. Applicant: Hewlett-Packard Co.. Device class: 2.
Clearance details
- Applicant
- Hewlett-Packard Co.
- 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
- Mchenry, IL, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.