THEOFAST(TM) TEST PACKAGE— 510(k) K863475
Substantially Equivalent3M Company
FDA 510(k) clearance K863475 for THEOFAST(TM) TEST PACKAGE, Substantially Equivalent on 1986-11-05. Applicant: 3M Company. Device class: 2.
Clearance details
- Applicant
- 3M Company
- Product code
- Code LER
- Device class
- Class 2
- Regulation
- 21 CFR 862.3880
- Advisory panel
- Clinical Toxicology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mountain View, CA, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.