Product code LHZ
- Device name
- Viscometer, Mucus, Cervical
- Medical specialty
- Obstetrics/Gynecology
- Device class
- 1
- Regulation number
- 884.1040
- Review panel
- OB
- Implant
- N
- Life sustaining/supporting
- N
- GMP exempt
- N
- Third party review
- N
- Summary malfunction reporting
- Eligible
- Source
- FDA openFDA device classification dataset
Related 510(k) Records
| 510(k) | Device | Applicant | Decision date |
|---|
| K936006 | SALTIME VISCOMETER | Harold J. Kosasky, M.D. | 1996-02-09 |
Related GUDID Devices
| Primary DI | Brand | Company | Published |
|---|
| 10192253007183 | Kangaroo | Cardinal Health 200, LLC | 2024-09-03 |