LIKON— 510(k) K881777
Substantially EquivalentNorthwood Intl., Corp.
FDA 510(k) clearance K881777 for LIKON, Substantially Equivalent on 1989-10-16. Applicant: Northwood Intl., Corp.. Device class: 2.
Clearance details
- Applicant
- Northwood Intl., Corp.
- Product code
- Code IPF
- Device class
- Class 2
- Regulation
- 21 CFR 890.5850
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- San Jose, CA, US
Recent devices under product code IPF
view allData sourced from openFDA. This site is unofficial and independent of the FDA.