K841652 is an FDA 510(k) clearance for the OCULAR PRESSURE APPLICATOR..
Submitted by The Lebanon Corp. (Mchenry, US). The FDA issued a Cleared decision on June 1, 1984, 42 days after receiving the submission on April 20, 1984.
This device falls under the Ophthalmic FDA review panel.
| 510(k) Number | K841652 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | April 20, 1984 |
| Decision Date | June 01, 1984 |
| Days to Decision | 42 days |
| Submission Type | Traditional |
| Review Panel | Ophthalmic (OP) |
| Summary | — |
| Product Code | — |
| Device Class | — |