LHZ — Viscometer, Mucus, Cervical Class I
FDA product code LHZ covers "Viscometer, Mucus, Cervical", a Class I medical device regulated under 21 CFR 884.1040. Submissions are reviewed by the Obstetrics/Gynecology panel. At least 1 recent 510(k) clearance has been granted under this product code.
Classification Details
- Product Code
- LHZ
- Device Class
- Class I
- Regulation Number
- 884.1040
- Submission Type
- Review Panel
- OB
- Medical Specialty
- Obstetrics/Gynecology
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|---|---|---|
| K936006 | harold j. kosasky, m.d | SALTIME VISCOMETER | February 9, 1996 |