REPLICA PLATER— 510(k) K810719
Substantially EquivalentDynatech Corp.
FDA 510(k) clearance K810719 for REPLICA PLATER, Substantially Equivalent on 1981-04-01. Applicant: Dynatech Corp..
Clearance details
- Applicant
- Dynatech Corp.
- Product code
- Code JTC
- Advisory panel
- Microbiology
- 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.