PERCUTANEOUS INTRODUCER FOR VENA CAVA FILTER SYST
FDA 510(k) clearance K932921 · decided 1993-08-30
Clearance details
- K-number
- K932921
- Device name
- PERCUTANEOUS INTRODUCER FOR VENA CAVA FILTER SYST
- Applicant
- B. Braun Vena-Tech
- Decision
- Substantially Equivalent
- Date received
- 1993-06-15
- Decision date
- 1993-08-30
- Days to decision
- 76 days
- Clearance type
- Traditional
- Product code
- DTK
- Device class
- 2
- Regulation number
- 870.3375
- Medical specialty
- Cardiovascular
- Advisory committee
- Cardiovascular
- Location
- Evanston, IL, US
- Third-party review
- No
- Expedited review
- No
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Similar devices under this product code
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Recalls involving this device
No recalls on record reference this clearance.