INTERCASSETTE, INTERKIT, UNIVERSAL PAK & CASSETTE — CooperVision, Inc. (510(k) K890300)
INTERCASSETTE, INTERKIT, UNIVERSAL PAK & CASSETTE — CooperVision, Inc. (510(k) K890300) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: INTERCASSETTE, INTERKIT, UNIVERSAL PAK & CASSETTE; Applicant: CooperVision, Inc.; Clearance track: 510(k).
| Device name | INTERCASSETTE, INTERKIT, UNIVERSAL PAK & CASSETTE |
|---|---|
| Applicant | CooperVision, Inc. |
| Clearance track | 510(k) |
| Submission number | K890300 |
| Decision | Substantially Equivalent |
| Decision date | 1989-04-17 |
| Date received | 1989-01-19 |
| Product code | HQE |
| Device class | 2 |
| Medical specialty | Ophthalmic |
| Applicant location | CA, US |
| Source | openFDA device |
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