THERMOVENT 600, 1200, T, 02— 510(k) K874597
Substantially EquivalentPortex, Inc.
FDA 510(k) clearance K874597 for THERMOVENT 600, 1200, T, 02, Substantially Equivalent on 1988-01-19. Applicant: Portex, Inc.. Device class: 1.
Clearance details
- Applicant
- Portex, Inc.
- Product code
- Code BYD
- Device class
- Class 1
- Regulation
- 21 CFR 868.5375
- Advisory panel
- Anesthesiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Wilmington, MA, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.