MODIFICATION TO BIOTRONIK'S STERILIZATION PROCESS
FDA 510(k) clearance K023803 · decided 2002-12-11
Clearance details
- K-number
- K023803
- Device name
- MODIFICATION TO BIOTRONIK'S STERILIZATION PROCESS
- Applicant
- Biotronik, Inc.
- Decision
- Substantially Equivalent
- Date received
- 2002-11-14
- Decision date
- 2002-12-11
- Days to decision
- 27 days
- Clearance type
- Special
- Product code
- DTB
- Device class
- 3
- Regulation number
- 870.3680
- Medical specialty
- Cardiovascular
- Advisory committee
- Cardiovascular
- Location
- Lake Oswego, OR, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.