KARL STORZ Endoscopy-America, Inc. · Class I · Cleared Apr 21, 2000
| K-number | K000212 |
| Device name | KSEA CHARDONNES MORCELLATION KNIFE |
| Applicant | KARL STORZ Endoscopy-America, Inc. |
| Product code | KOH |
| Device class | Class I |
| Decision date | Apr 21, 2000 |
| Decision | Substantially Equivalent |
| Regulation | 884.4520 |
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