DETERM. SIZE 72 RADIAL-HUMAN IGD— 510(k) K831956
Substantially EquivalentKent Laboratories, Inc.
FDA 510(k) clearance K831956 for DETERM. SIZE 72 RADIAL-HUMAN IGD, Substantially Equivalent on 1983-07-18. Applicant: Kent Laboratories, Inc..
Clearance details
- Applicant
- Kent Laboratories, Inc.
- Product code
- Code CZJ
- Advisory panel
- Immunology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.