K873470 is an FDA 510(k) clearance for the TEMPLATE. This device is classified as a Tape, Measuring, Rulers And Calipers (Class I - General Controls, product code FTY).
Submitted by Cox-Uphuff Intl. (Santa Barbara, US). The FDA issued a Cleared decision on September 8, 1987, 11 days after receiving the submission on August 28, 1987.
This device falls under the General & Plastic Surgery FDA review panel. Regulated under 21 CFR 878.4800.
| 510(k) Number | K873470 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | August 28, 1987 |
| Decision Date | September 08, 1987 |
| Days to Decision | 11 days |
| Submission Type | Traditional |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | — |
| Product Code | FTY — Tape, Measuring, Rulers And Calipers |
| Device Class | Class I - General Controls |
| CFR Regulation | 21 CFR 878.4800 |