CRITIKON #817 ESOPHAGEAL MULTI-PROBE— 510(k) K821890
Substantially EquivalentCritikon Company, LLC
FDA 510(k) clearance K821890 for CRITIKON #817 ESOPHAGEAL MULTI-PROBE, Substantially Equivalent on 1982-08-03. Applicant: Critikon Company, LLC.
Clearance details
- Applicant
- Critikon Company, LLC
- Product code
- Code BZT
- Advisory panel
- Anesthesiology
- 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.