LHZ
1 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Viscometer, Mucus, Cervical
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 884.1040
- Medical specialty
- Obstetrics/Gynecology
- Adverse events (MAUDE)
- 1995: 1
Reports received by FDA, not confirmed device causation - volume tracks device popularity as much as risk.
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| Record | Firm | Date | Builder |
|---|---|---|---|
| SALTIME VISCOMETER (K936006) | Harold J. Kosasky, M.D. | 1996-02-09 | + Add |
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Every clearance here is in the API, with alerts when new ones post.