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FDA 510(k), K936006, SALTIME VISCOMETER
FDA 510(k), K936006, SALTIME VISCOMETER
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510(K) Number: K936006
Device Name: SALTIME VISCOMETER
Manufacturer: HAROLD J. KOSASKY, M.D.
Device Classification Name: viscometer, mucus, cervical
Regulation Number: 884.1040
Classification Product Code: LHZ
Date Received: 12/15/1993
Decision Date: 02/09/1996
Regulation Medical Specialty: Obstetrics/Gynecology
Device Name: SALTIME VISCOMETER
Manufacturer: HAROLD J. KOSASKY, M.D.
Device Classification Name: viscometer, mucus, cervical
Regulation Number: 884.1040
Classification Product Code: LHZ
Date Received: 12/15/1993
Decision Date: 02/09/1996
Regulation Medical Specialty: Obstetrics/Gynecology
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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