Allergan, Inc. · Class I · Cleared May 29, 1987
| K-number | K870807 |
| Device name | BKS-1000 REFRACTIVE SET USE IN KERATOREFRACTIVE |
| Applicant | Allergan, Inc. |
| Product code | HNO |
| Device class | Class I |
| Decision date | May 29, 1987 |
| Decision | Substantially Equivalent |
| Regulation | 886.4370 |
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