K871213 is an FDA 510(k) clearance for the KUMAR CERVICAL APPLICATOR. This device is classified as a System, Applicator, Radionuclide, Manual (Class I - General Controls, product code IWJ).
Submitted by Mick Radio-Nuclear Instruments, Inc. (Bronx, US). The FDA issued a Cleared decision on July 16, 1987, 112 days after receiving the submission on March 26, 1987.
This device falls under the Radiology FDA review panel. Regulated under 21 CFR 892.5650.
| 510(k) Number | K871213 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | March 26, 1987 |
| Decision Date | July 16, 1987 |
| Days to Decision | 112 days |
| Submission Type | Traditional |
| Review Panel | Radiology (RA) |
| Summary | — |
| Product Code | IWJ — System, Applicator, Radionuclide, Manual |
| Device Class | Class I - General Controls |
| CFR Regulation | 21 CFR 892.5650 |