DIF-STET— 510(k) K832882
Substantially EquivalentIntersect Systems, Inc.
FDA 510(k) clearance K832882 for DIF-STET, Substantially Equivalent on 1983-12-06. Applicant: Intersect Systems, Inc.. Device class: 2.
Clearance details
- Applicant
- Intersect Systems, Inc.
- Product code
- Code DQD
- Device class
- Class 2
- Regulation
- 21 CFR 870.1875
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
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