Submission Details
| 510(k) Number | K864325 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | November 03, 1986 |
| Decision Date | November 19, 1986 |
| Days to Decision | 16 days |
| Submission Type | Traditional |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | — |
K864325 is an FDA 510(k) clearance for the DR7700 OPERATING TABLE, a Table, Operating-room, Ac-powered (Class I — General Controls, product code FQO), submitted by Koken Mfg Company, Inc. (St. Louis, US). The FDA issued a Cleared decision on November 19, 1986, 16 days after receiving the submission on November 3, 1986. This device falls under the General & Plastic Surgery review panel. Regulated under 21 CFR 878.4960.
| 510(k) Number | K864325 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | November 03, 1986 |
| Decision Date | November 19, 1986 |
| Days to Decision | 16 days |
| Submission Type | Traditional |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | — |
| Product Code | FQO — Table, Operating-room, Ac-powered |
| Device Class | Class I — General Controls |
| CFR Regulation | 21 CFR 878.4960 |