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.. Device class: 2.
Clearance details
- Applicant
- Seismed Instruments, Inc.
- Product code
- Code DSB
- Device class
- Class 2
- Regulation
- 21 CFR 870.2770
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Minneapolis, MN, US
Recent devices under product code DSB
view allMore clearances from Seismed Instruments, Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.