Product code DID— Clinical Toxicology

FDA has cleared 5 devices under product code DID between 1978 and 1982, filed by 5 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.

• 19821 clearance
• 19801 clearance
• 19783 clearances

• Syva Co.1 clearance
• Nichols Institute Diagnostics1 clearance
• New England Nuclear1 clearance
• Monitor Science Corp.1 clearance
• Beckman Instruments, Inc.1 clearance

• K820773 — EMIT-ST URINE COCAINE METABOLITE ASSAYSyva Co.·1982-04-08
• K802038 — PHENYTOIN REAGENT TEST KITBeckman Instruments, Inc.·1980-10-23
• K780950 — BIO-MONITOR TOBRAMYCINMonitor Science Corp.·1978-08-14
• K780182 — TOBRAMYCIN 125I RIA KITNew England Nuclear·1978-02-13
• K780048 — AMINOGLYCOSIDE TEST SYSTEMNichols Institute Diagnostics·1978-01-20