Concord Laboratories, Inc. · Class I · Cleared Dec 27, 1983
| K-number | K833582 |
| Device name | PULSATOR ARTERIAL BLOOD SAMPLING SYRIN |
| Applicant | Concord Laboratories, Inc. |
| Product code | CBT |
| Device class | Class I |
| Decision date | Dec 27, 1983 |
| Decision | Substantially Equivalent |
| Regulation | 868.1100 |
AI extraction for this record is queued and will appear within 24 hours. View full FDA record →
View the full FDA submission: accessdata.fda.gov