LIGHTNING DIALYZER— 510(k) K810871
Substantially EquivalentClintox Laboratories, Inc.
FDA 510(k) clearance K810871 for LIGHTNING DIALYZER, Substantially Equivalent on 1981-07-10. Applicant: Clintox Laboratories, Inc.. Device class: 1.
Clearance details
- Applicant
- Clintox Laboratories, Inc.
- Product code
- Code DHY
- Device class
- Class 1
- Regulation
- 21 CFR 866.5065
- 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.