Aggrecetin
510(k) K760893
Aggrecetin is a Class II device made by Bio/Data Corp., cleared under FDA 510(k) K760893 on 12 Jan 1977, active as of 10 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK760893 | Date12 Jan 1977 | StatusActive |
Official records
- FDA 510(k) database K760893
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- JOZ
- Device class
- Class II
- Regulation
- 21 CFR Part 864.5700
- Advisory committee
- Hematology
- FDA decision
- SESE Substantially Equivalent
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- Chrono-Log Whole Blood Lumi-Aggregometer Model 700 by CHRONO-LOG CORP