SEISMOCARDIOGRAPH - SCG(TM) 1000 SERIES— 510(k) K892323
Substantially EquivalentSeismed Instruments, Inc.
FDA 510(k) clearance K892323 for SEISMOCARDIOGRAPH - SCG(TM) 1000 SERIES, Substantially Equivalent on 1989-10-30. Applicant: Seismed Instruments, Inc..
Clearance details
- Applicant
- Seismed Instruments, Inc.
- Product code
- Code DSB
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Minneapolis, MN, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.