Hgm, Inc. · Class II · Cleared Aug 25, 1987
| K-number | K872630 |
| Device name | ENDOCOAGULATOR(TM) MODEL 20 ARGON LASER FOR UROLO. |
| Applicant | Hgm, Inc. |
| Product code | LNK |
| Device class | Class II |
| Decision date | Aug 25, 1987 |
| Decision | Substantially Equivalent |
| Regulation | 878.4810 |
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