WESCO BLANKET
FDA 510(k) clearance K981093 · decided 2000-03-28
Clearance details
- K-number
- K981093
- Device name
- WESCO BLANKET
- Applicant
- Wesco, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1998-03-26
- Decision date
- 2000-03-28
- Days to decision
- 733 days
- Clearance type
- Traditional
- Product code
- DWJ
- Device class
- 2
- Regulation number
- 870.5900
- Medical specialty
- Cardiovascular
- Advisory committee
- Cardiovascular
- Location
- East Peoria, IL, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.