K844757 is an FDA 510(k) clearance for the TUBING HOLDER..
Submitted by Procter & Gamble Mfg. Co. (Cincinnati, US). The FDA issued a Cleared decision on December 17, 1984, 10 days after receiving the submission on December 7, 1984.
This device falls under the General & Plastic Surgery FDA review panel.
| 510(k) Number | K844757 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | December 07, 1984 |
| Decision Date | December 17, 1984 |
| Days to Decision | 10 days |
| Submission Type | Traditional |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | — |
| Product Code | — |
| Device Class | — |