Product code IDO— Pathology

FDA has cleared 5 devices under product code IDO between 1981 and 1987, filed by 3 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.

• 19871 clearance
• 19861 clearance
• 19841 clearance
• 19812 clearances

• Lkb Instruments, Inc.3 clearances
• Surgipath Medical Industries, Inc.1 clearance
• Miles Laboratories, Inc.1 clearance

• K864733 — LKB 2260 MACROTOMELkb Instruments, Inc.·1987-01-05
• K863548 — ROTARY MICROTOMESurgipath Medical Industries, Inc.·1986-09-19
• K843505 — LKB 2230 ROTARY ONELkb Instruments, Inc.·1984-11-30
• K812558 — TISSUE-TEK III ACCU-CUT ROTARY MICROTOMEMiles Laboratories, Inc.·1981-09-29
• K812157 — LKB-BROMMA 2218 HISTORANGE MICROTOMELkb Instruments, Inc.·1981-08-18