510(k) K930823
K930823 is an FDA 510(k) premarket notification submitted by Diagnostic Specialties for the device "PROTEIN-BOUND GLUCOSE ASSAYN KIT". The FDA issued a decision of Substantially Equivalent on August 19, 1993. The device falls under product code LCP (Assay, Glycosylated Hemoglobin), a Class II device regulated under 21 CFR 864.7470. Diagnostic Specialties has at least 7 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 19, 1993
- Date Received
- February 17, 1993
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Assay, Glycosylated Hemoglobin
- Device Class
- Class II
- Regulation Number
- 864.7470
- Review Panel
- HE
- Submission Type