Product code LFQ— Clinical Chemistry

FDA has cleared 5 devices under product code LFQ between 1981 and 1986, filed by 5 applicant companies. No FDA device recalls reference this product code. Class I devices are low-risk and subject to FDA general controls; many Class I device types are exempt from 510(k) premarket notification.

• 19862 clearances
• 19841 clearance
• 19812 clearances

• Technostics Intl.1 clearance
• Sterling Diagnostics, Inc.1 clearance
• Sandare Chemical Co., Inc.1 clearance
• Livonia Diagnostics, Inc.1 clearance
• Anco Medical Reagents & Assoc.1 clearance

• K860111 — URIC ACID REAGENT SETTechnostics Intl.·1986-02-19
• K860142 — URIC ACID REAGENT SET (COLORIMETRIC)Sterling Diagnostics, Inc.·1986-02-11
• K844075 — URIC ACID REAGENT SETLivonia Diagnostics, Inc.·1984-10-30
• K812313 — SANDARE URIC ACID PROCEDURESandare Chemical Co., Inc.·1981-09-01
• K811764 — URIC ACID REAGENT SETAnco Medical Reagents & Assoc.·1981-08-20