RHINOTEST MP— 510(k) K853024
Substantially EquivalentIntertronic, Inc.
FDA 510(k) clearance K853024 for RHINOTEST MP, Substantially Equivalent on 1985-09-27. Applicant: Intertronic, Inc.. Device class: 2.
Clearance details
- Applicant
- Intertronic, Inc.
- Product code
- Code BXQ
- Device class
- Class 2
- Regulation
- 21 CFR 868.1800
- Advisory panel
- Anesthesiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Scottsdale, AZ, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.