510(k) K943550
K943550 is an FDA 510(k) premarket notification submitted by Sigma Diagnostics, Inc. for the device "GENTAMICIN FPIA REAGENT SET AND CALIBRATORS". The FDA issued a decision of Substantially Equivalent on November 17, 1994. The device falls under product code LCQ (Fluorescent Immunoassay Gentamicin), a Class II device regulated under 21 CFR 862.3450. Sigma Diagnostics, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- November 17, 1994
- Date Received
- July 21, 1994
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Fluorescent Immunoassay Gentamicin
- Device Class
- Class II
- Regulation Number
- 862.3450
- Review Panel
- TX
- Submission Type