PURITAN BENNETT PB900A DIAGNOSTIC SPIROMETER— 510(k) K890522
Substantially EquivalentPuritan Bennett Corp.
FDA 510(k) clearance K890522 for PURITAN BENNETT PB900A DIAGNOSTIC SPIROMETER, Substantially Equivalent on 1989-04-21. Applicant: Puritan Bennett Corp.. Device class: 2.
Clearance details
- Applicant
- Puritan Bennett Corp.
- Product code
- Code BZG
- Device class
- Class 2
- Regulation
- 21 CFR 868.1840
- 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.