510(k) K920767
K920767 is an FDA 510(k) premarket notification submitted by Nycomed Pharma AS for the device "NYCOPLASTIN". The FDA issued a decision of Substantially Equivalent on Feb 12, 1993. The device falls under product code GJS (Test, Time, Prothrombin), a Class II device regulated under 21 CFR 864.7750.
Clearance details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Feb 12, 1993
- Date Received
- Feb 19, 1992
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device classification
- Device Name
- Test, Time, Prothrombin
- Device Class
- Class II
- Regulation Number
- 864.7750
- Review Panel
- HE
- Submission Type
- 510(k)