510(k) K994073
K994073 is an FDA 510(k) premarket notification submitted by Gds Technology, LLC for the device "HEMOSITE TEST SYSTEM". The FDA issued a decision of Substantially Equivalent on January 14, 2000. The device falls under product code KHG (Whole Blood Hemoglobin Determination), a Class II device regulated under 21 CFR 864.7500. Gds Technology, LLC has at least 7 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 14, 2000
- Date Received
- December 2, 1999
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Whole Blood Hemoglobin Determination
- Device Class
- Class II
- Regulation Number
- 864.7500
- Review Panel
- HE
- Submission Type