HDF — Speculum, Vaginal, Metal Class I
FDA Device Classification
Classification Details
- Product Code
- HDF
- Device Class
- Class I
- Regulation Number
- 884.4520
- Submission Type
- Review Panel
- OB
- Medical Specialty
- Obstetrics/Gynecology
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|
| K926429 | thomasville medical assoc | VAGINAL SPECULA: CUSCO, GUTTMAN, INFANT | February 28, 1994 |
| K902019 | gynescope | MODIFIED METAL SPECULUM & SPECIAL BULLET FORCEPS | June 7, 1990 |
| K891041 | zinnanti surgical instruments | MIYA SPECULUM | March 22, 1989 |
| K891044 | zinnanti surgical instruments | LASER SPECULA | March 17, 1989 |
| K890375 | kinetic medical products | VAGINAL SPECULUM | February 13, 1989 |
| K862478 | franklin medical usa | HAYES VAGINAL SHIELD | November 24, 1986 |
| K853640 | downs surgical | WELLINGTON HOSPITAL PATTERN SELF RETAINING VAGINAL | October 29, 1985 |
| K851799 | artiberia | 61-100 TO 61-124 VARIOUS VAGINAL SPECVIA(CUSCO,GRA | May 22, 1985 |
| K843388 | downs surgical | WELLINGTON HOSPITAL PATTERN SELF-RETAIN | October 1, 1984 |
| K821297 | conphar | GRAVES SPECULA | May 24, 1982 |
| K821291 | conphar | PEDERSON VAGINAL SPECULA | May 24, 1982 |