510(k) K895262
K895262 is an FDA 510(k) premarket notification submitted by Medical Diagnostic Technologies, Inc. for the device "NORMAL COAGULATION CONTROL PLASMA (NCCP)". The FDA issued a decision of Substantially Equivalent on October 6, 1989. The device falls under product code GIZ (Plasma, Control, Normal), a Class II device regulated under 21 CFR 864.5425. Medical Diagnostic Technologies, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- October 6, 1989
- Date Received
- August 22, 1989
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Plasma, Control, Normal
- Device Class
- Class II
- Regulation Number
- 864.5425
- Review Panel
- HE
- Submission Type