510(k) K982003
K982003 is an FDA 510(k) premarket notification submitted by Drew Scientific , Ltd. for the device "DS30 HCY HOMOCYSTEINE ASSAY KIT". The FDA issued a decision of Substantially Equivalent on February 11, 1999. The device falls under product code LPS (Urinary Homocystine (Nonquantitative) Test System), a Class II device regulated under 21 CFR 862.1377. Drew Scientific , Ltd. has at least 8 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- February 11, 1999
- Date Received
- June 8, 1998
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Urinary Homocystine (Nonquantitative) Test System
- Device Class
- Class II
- Regulation Number
- 862.1377
- Review Panel
- CH
- Submission Type