NEOSERV 824
FDA 510(k) clearance K900729 · decided 1990-06-08
Clearance details
- K-number
- K900729
- Device name
- NEOSERV 824
- Applicant
- Burdick Corp.
- Decision
- Substantially Equivalent
- Date received
- 1990-02-15
- Decision date
- 1990-06-08
- Days to decision
- 113 days
- Clearance type
- Traditional
- Product code
- MCJ
- Advisory committee
- Unknown
- Location
- Miltoon, WI, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.