K883867 is an FDA 510(k) clearance for the CERVICAL BIOPSY INSTRUMENT. This device is classified as a Tampon, Menstrual, Unscented (Class II - Special Controls, product code HEB).
Submitted by Mend Technologies, Inc. (Dallas, US). The FDA issued a Cleared decision on November 29, 1988, 77 days after receiving the submission on September 13, 1988.
This device falls under the Obstetrics & Gynecology FDA review panel. Regulated under 21 CFR 884.5470. An Unscented Menstrual Tampon Is A Plug Made Of Cellulosic Or Synthetic Material That Is Inserted Into The Vagina And Used To Absorb Menstrual Fluid Or Other Vaginal Discharge..
| 510(k) Number | K883867 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | September 13, 1988 |
| Decision Date | November 29, 1988 |
| Days to Decision | 77 days |
| Submission Type | Traditional |
| Review Panel | Obstetrics & Gynecology (OB) |
| Summary | — |
| Product Code | HEB — Tampon, Menstrual, Unscented |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 884.5470 |
| Definition | An Unscented Menstrual Tampon Is A Plug Made Of Cellulosic Or Synthetic Material That Is Inserted Into The Vagina And Used To Absorb Menstrual Fluid Or Other Vaginal Discharge. |