Oec-Diasonics, Inc.

Oec-Diasonics, Inc. holds 8 FDA 510(k) medical device clearances, first cleared 1985, most recent 1993.

Top product codes for Oec-Diasonics, Inc.

Recent clearances by Oec-Diasonics, Inc.

K926056 — 9600 FLUOROSCOPIC IMAGING SYSTEMCode OXO·1993-01-21
K924879 — EP 3000Code JAA·1993-01-04
K914446 — UROVIEW 2000, MODIFICATIONCode JAA·1992-01-10
K896583 — F.A.S.T. TABLECode IXR·1990-03-01
K893475 — UROVIEW IICode JAA·1989-08-10
K872022 — UROVIEWCode KQS·1987-07-16
K864837 — MODIFIED MAINFRAME OF MODEL 902 MOBILE C-ARMCode JAA·1987-01-30
K843972 — ANGIOPLUS-SCode JAA·1985-01-03

Data sourced from openFDA. This site is unofficial and independent of the FDA.