PULSE CRP TEST— 510(k) K923768
Substantially EquivalentPulse Scientific, Inc.
FDA 510(k) clearance K923768 for PULSE CRP TEST, Substantially Equivalent on 1992-12-01. Applicant: Pulse Scientific, Inc..
Clearance details
- Applicant
- Pulse Scientific, Inc.
- Product code
- Code DCK
- Advisory panel
- Immunology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Burlington, Ont., Canada, CA
Data sourced from openFDA. This site is unofficial and independent of the FDA.