Veronal Buffer
510(k) K761171
Veronal Buffer is a Class II device made by Bio/Data Corp., cleared under FDA 510(k) K761171 on 10 Jan 1977, active as of 22 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 | NumberK761171 | Date10 Jan 1977 | StatusActive |
Official records
- FDA 510(k) database K761171
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- JPA
- Device class
- Class II
- Regulation
- 21 CFR Part 864.5425
- Advisory committee
- Hematology
- FDA decision
- SESE Substantially Equivalent
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