VERSA-VIAL
Device Facts
| Record ID | K920177 |
|---|---|
| Device Name | VERSA-VIAL |
| Applicant | Bioteque America, Inc. |
| Product Code | DQF · Cardiovascular |
| Decision Date | Jul 13, 1992 |
| Decision | SESE |
| Submission Type | Traditional |
| Regulation | 21 CFR 870.1670 |
| Device Class | Class 2 |
| Record ID | K920177 |
|---|---|
| Device Name | VERSA-VIAL |
| Applicant | Bioteque America, Inc. |
| Product Code | DQF · Cardiovascular |
| Decision Date | Jul 13, 1992 |
| Decision | SESE |
| Submission Type | Traditional |
| Regulation | 21 CFR 870.1670 |
| Device Class | Class 2 |
Predicate graph will load when search results are available.
Embedding visualization will load when search results are available.
PDF viewer will load when search results are available.
Select an item from Submissions
Click any panel, subpart, regulation, product code, or device to see details here.
Loading collections...