ALBUMIN
FDA 510(k) clearance K771828 · decided 1977-10-25
Clearance details
- K-number
- K771828
- Device name
- ALBUMIN
- Applicant
- Gamma Enterprises, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1977-09-29
- Decision date
- 1977-10-25
- Days to decision
- 26 days
- Clearance type
- Traditional
- Product code
- CIX
- Device class
- 2
- Regulation number
- 862.1035
- 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.