Submission Details
| 510(k) Number | K831039 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | March 31, 1983 |
| Decision Date | May 27, 1983 |
| Days to Decision | 57 days |
| Submission Type | Traditional |
| Review Panel | Dental (DE) |
| Summary | — |
K831039 is an FDA 510(k) clearance for the COMPLUS VARIOUS FORMS, submitted by Parker Laboratories, Inc. (Mchenry, US). The FDA issued a Cleared decision on May 27, 1983, 57 days after receiving the submission on March 31, 1983. This device falls under the Dental review panel.
| 510(k) Number | K831039 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | March 31, 1983 |
| Decision Date | May 27, 1983 |
| Days to Decision | 57 days |
| Submission Type | Traditional |
| Review Panel | Dental (DE) |
| Summary | — |
| Product Code | — |
| Device Class | — |