MODIFIED SEISMOCARDIOGRAPH— 510(k) K910994
Substantially EquivalentSeismed Instruments, Inc.
FDA 510(k) clearance K910994 for MODIFIED SEISMOCARDIOGRAPH, Substantially Equivalent on 1992-01-15. 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
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