510(k) K823558
K823558 is an FDA 510(k) premarket notification submitted by Fisher Scientific Co., LLC for the device "MICRO-HEMATOCRIT CENTRIFUGE 335/336". The FDA issued a decision of Substantially Equivalent on January 21, 1983. The device falls under product code JPI (Device, Hematocrit Measuring), a Class II device regulated under 21 CFR 864.6400. Fisher Scientific Co., LLC has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 21, 1983
- Date Received
- December 2, 1982
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Device, Hematocrit Measuring
- Device Class
- Class II
- Regulation Number
- 864.6400
- Review Panel
- HE
- Submission Type