MODIFICATION TO RELIEF BRIEF— 510(k) K003128
Substantially EquivalentThe JM Kohn Co.
FDA 510(k) clearance K003128 for MODIFICATION TO RELIEF BRIEF, Substantially Equivalent on 2002-08-12. Applicant: The JM Kohn Co.. Device class: 1.
Clearance details
- Applicant
- The JM Kohn Co.
- Product code
- Code NJB
- Device class
- Class 1
- Regulation
- 21 CFR 890.3490
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- San Francisco, CA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.