SPECIMEN COLLECTOR— 510(k) K770112
Substantially EquivalentPortex, Inc.
FDA 510(k) clearance K770112 for SPECIMEN COLLECTOR, Substantially Equivalent on 1977-03-14. Applicant: Portex, Inc.. Device class: 1.
Clearance details
- Applicant
- Portex, Inc.
- Product code
- Code FMH
- Device class
- Class 1
- Regulation
- 21 CFR 864.3250
- Advisory panel
- Pathology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Walker, MI, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.