CDI(TM) 2000 BLOOD GAS MONITORING SYST, MODIFIED— 510(k) K912030
Substantially Equivalent3M Company
FDA 510(k) clearance K912030 for CDI(TM) 2000 BLOOD GAS MONITORING SYST, MODIFIED, Substantially Equivalent on 1991-10-30. Applicant: 3M Company. Device class: 2.
Clearance details
- Applicant
- 3M Company
- Product code
- Code CBZ
- Device class
- Class 2
- Regulation
- 21 CFR 868.1170
- Advisory panel
- Anesthesiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Tustin, CA, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.