510(k) K936006
- Device
- SALTIME VISCOMETER
- Applicant
- HAROLD J. KOSASKY, M.D.
- 510(k) number
- K936006
- Product code
- LHZ
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1996-02-09
- Date received
- 1993-12-15
- Regulation
- 884.1040
- Classification name
- Viscometer, Mucus, Cervical
- Medical specialty
- Obstetrics/Gynecology
- Review panel
- Obstetrics/Gynecology
- Device class
- 1
- Clearance type
- Traditional
- Statement or summary
- Summary
- Third party reviewed
- No
Related Records
Applicant Contact
- Contact
- HAROLD J KOSASKY
- Address
- 25 Boylston St. Chestnut Hill MA US 02167 02167
Source Documents
Legacy Summary
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FDA Review
Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links Follow FDA En Español Home Food Drugs Medical Devices Radiation-Emitting Products Vaccines, Blood & Biologics Animal & Veterinary Cosmetics Tobacco Products FDA Home Medical Devices Databases