Submission Details
| 510(k) Number | K822208 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | July 23, 1982 |
| Decision Date | August 27, 1982 |
| Days to Decision | 35 days |
| Submission Type | Traditional |
| Review Panel | Chemistry (CH) |
| Summary | — |
K822208 is an FDA 510(k) clearance for the CAVRO IQ-190 SAMPLE PROCESSOR, a Station, Pipetting And Diluting, For Clinical Use (Class I — General Controls, product code JQW), submitted by Cavro Scientific Instruments, Inc. (Walker, US). The FDA issued a Cleared decision on August 27, 1982, 35 days after receiving the submission on July 23, 1982. This device falls under the Chemistry review panel. Regulated under 21 CFR 862.2750.
| 510(k) Number | K822208 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | July 23, 1982 |
| Decision Date | August 27, 1982 |
| Days to Decision | 35 days |
| Submission Type | Traditional |
| Review Panel | Chemistry (CH) |
| Summary | — |
| Product Code | JQW — Station, Pipetting And Diluting, For Clinical Use |
| Device Class | Class I — General Controls |
| CFR Regulation | 21 CFR 862.2750 |