HFC — Aspirator, Endocervical Class II
FDA Device Classification
Classification Details
- Product Code
- HFC
- Device Class
- Class II
- Regulation Number
- 884.1050
- Submission Type
- Review Panel
- OB
- Medical Specialty
- Obstetrics/Gynecology
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|
| K974032 | a and a medical | ROCKET MUCUS SAMPLER SYRINGE, STERILE, ROCKET MUCUS SAMPLER SYRINGE, CLINICALLY | December 22, 1997 |
| K960263 | cook urological | CERVICAL MUCOUS ASPIRATION CATHETER | August 29, 1996 |
| K954903 | cook urological | PEDI VAGINAL ASPIRATOR | April 29, 1996 |
| K954102 | select medical systems | SELECTMUCUS | November 21, 1995 |
| K902242 | innovative medical products | ENDOCERVICAL ASPIRATOR | October 9, 1990 |
| K902032 | customed | O. B. PACK IV | September 28, 1990 |
| K902954 | permobil | OBER2 MONITOR, EYE MOVEMENT (OPHTHALMIC) | August 23, 1990 |
| K895403 | unimar | ASPIRETTE ENDOCERVICAL ASPIRATOR | November 29, 1989 |
| K821134 | seamless hospital products | DC PACK TM | June 22, 1982 |
| K812175 | fertility instrumentation | ENDOCERVICAL ASPIRATOR | September 21, 1981 |
| K801238 | robert hasselbrack, m.d | ACCU-PAP T ZONE SAMPLER | August 12, 1980 |