Penny & Giles Blackwood , Ltd. · Class I · Cleared Dec 19, 1988
| K-number | K884003 |
| Device name | GONIOMETER AND BIOMEDICAL RECORDER SYSTEM |
| Applicant | Penny & Giles Blackwood , Ltd. |
| Product code | KQX |
| Device class | Class I |
| Decision date | Dec 19, 1988 |
| Decision | Substantially Equivalent |
| Regulation | 888.1500 |
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