PB3200 INTRA-ARTERIAL BLOOD GAS MONITORING SYSTEM— 510(k) K905397
Substantially EquivalentPuritan Bennett Corp.
FDA 510(k) clearance K905397 for PB3200 INTRA-ARTERIAL BLOOD GAS MONITORING SYSTEM, Substantially Equivalent on 1991-05-14. Applicant: Puritan Bennett Corp.. Device class: 2.
Clearance details
- Applicant
- Puritan Bennett Corp.
- Product code
- Code CCE
- Device class
- Class 2
- Regulation
- 21 CFR 868.1200
- Advisory panel
- Anesthesiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Overland Park, KS, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.