TIMEOSCOPE AND FLEXISCOPE— 510(k) K924095
Substantially EquivalentStethoscopes of America, Inc.
FDA 510(k) clearance K924095 for TIMEOSCOPE AND FLEXISCOPE, Substantially Equivalent on 1992-10-20. Applicant: Stethoscopes of America, Inc..
Clearance details
- Applicant
- Stethoscopes of America, Inc.
- Product code
- Code LDE
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Stone Mountain, GA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.