K823040 is an FDA 510(k) clearance for the PATHOLOGY INSTRUMENTATION & ACCESSORIES. This device is classified as a Light, Microscope (Class I - General Controls, product code IBJ).
Submitted by Iris Remote Imaging Systems (Mchenry, US). The FDA issued a Cleared decision on January 14, 1983, 92 days after receiving the submission on October 14, 1982.
This device falls under the Pathology FDA review panel. Regulated under 21 CFR 864.3600.
| 510(k) Number | K823040 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | October 14, 1982 |
| Decision Date | January 14, 1983 |
| Days to Decision | 92 days |
| Submission Type | Traditional |
| Review Panel | Pathology (PA) |
| Summary | — |
| Product Code | IBJ — Light, Microscope |
| Device Class | Class I - General Controls |
| CFR Regulation | 21 CFR 864.3600 |