Harvey-Bostwick, Inc. · Class II · Cleared Aug 24, 1982
| K-number | K821942 |
| Device name | HARVEY-BOSTWICK BRADY CARDIA MONIT. HB85 |
| Applicant | Harvey-Bostwick, Inc. |
| Product code | DRT |
| Device class | Class II |
| Decision date | Aug 24, 1982 |
| Decision | Substantially Equivalent |
| Regulation | 870.2300 |
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