VELCOM-100
FDA 510(k) clearance K863210 · decided 1986-11-26
Clearance details
- K-number
- K863210
- Device name
- VELCOM-100
- Applicant
- Waters Instruments, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1986-08-20
- Decision date
- 1986-11-26
- Days to decision
- 98 days
- Clearance type
- Traditional
- Product code
- DPW
- Device class
- 2
- Regulation number
- 870.2100
- Medical specialty
- Cardiovascular
- Advisory committee
- Cardiovascular
- Location
- Rochester, MN, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.