MULTI-CELL ULTRAFILTRATION SYSTEM
FDA 510(k) clearance K761100 · decided 1976-12-06
Clearance details
- K-number
- K761100
- Device name
- MULTI-CELL ULTRAFILTRATION SYSTEM
- Applicant
- Amicon, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1976-11-23
- Decision date
- 1976-12-06
- Days to decision
- 13 days
- Clearance type
- Traditional
- Product code
- JQQ
- Device class
- 1
- Regulation number
- 862.2050
- Medical specialty
- Clinical Chemistry
- Advisory committee
- Clinical Chemistry
- Location
- Mchenry, IL, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.