DIACYTE FIXATIVE SOLUTION— 510(k) K880549
Substantially EquivalentCytocorp, Inc.
FDA 510(k) clearance K880549 for DIACYTE FIXATIVE SOLUTION, Substantially Equivalent on 1988-04-01. Applicant: Cytocorp, Inc.. Device class: 1.
Clearance details
- Applicant
- Cytocorp, Inc.
- Product code
- Code LDY
- Device class
- Class 1
- Regulation
- 21 CFR 864.4010
- Advisory panel
- Pathology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Cleveland, OH, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.