Product code DOY— Clinical Toxicology

FDA has cleared 5 devices under product code DOY between 1983 and 1991, filed by 4 applicant companies. No FDA device recalls reference this product code. Class II devices are moderate-risk and subject to general and special controls; most reach market through 510(k) clearance by demonstrating substantial equivalence to a predicate device.

• 19911 clearance
• 19834 clearances

• Medrad, Inc.2 clearances
• Medical Parameters, Inc.1 clearance
• Gish Biomedical, Inc.1 clearance
• C.R. Bard, Inc.1 clearance

• K910154 — USCI ILLUMEN-8 8F PTCA GUIDING CATHETERC.R. Bard, Inc.·1991-04-09
• K832396 — CENTRAL VENOUS ACCESS CATHETER CVACGish Biomedical, Inc.·1983-08-31
• K831239 — WALRUS PERCUTANEOUS INTRODUCER SETMedical Parameters, Inc.·1983-05-25
• K831188 — CONNECTOR TUBEMedrad, Inc.·1983-05-09
• K831191 — VASCULAR CATHETERMedrad, Inc.·1983-05-09