MODIFICATION OF CRIT-LINE MONITOR III (CLM III)— 510(k) K982412
Substantially EquivalentIn-Line Diagnostics Corp.
FDA 510(k) clearance K982412 for MODIFICATION OF CRIT-LINE MONITOR III (CLM III), Substantially Equivalent on 1998-10-09. Applicant: In-Line Diagnostics Corp..
Clearance details
- Applicant
- In-Line Diagnostics Corp.
- Product code
- Code MQS
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Farmington, UT, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.