Submission Details
| 510(k) Number | K834577 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | December 29, 1983 |
| Decision Date | May 22, 1984 |
| Days to Decision | 145 days |
| Submission Type | Traditional |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | — |
K834577 is an FDA 510(k) clearance for the I/A PROBE LINES, submitted by Frigitronics of Connecticut, Inc. (Walker, US). The FDA issued a Cleared decision on May 22, 1984, 145 days after receiving the submission on December 29, 1983. This device falls under the General & Plastic Surgery review panel.
| 510(k) Number | K834577 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | December 29, 1983 |
| Decision Date | May 22, 1984 |
| Days to Decision | 145 days |
| Submission Type | Traditional |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | — |
| Product Code | — |
| Device Class | — |