INTERFACE MODULE IDDD
FDA 510(k) clearance K992635 · decided 1999-12-20
Clearance details
- K-number
- K992635
- Device name
- INTERFACE MODULE IDDD
- Applicant
- Stoeckert Instrumente
- Decision
- Substantially Equivalent
- Date received
- 1999-08-06
- Decision date
- 1999-12-20
- Days to decision
- 136 days
- Clearance type
- Special
- Product code
- KRI
- Device class
- 1
- Regulation number
- 870.4200
- Medical specialty
- Cardiovascular
- Advisory committee
- Cardiovascular
- Location
- North Attleboro, MA, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.