Cutler Laboratories, Inc.

Cutler Laboratories, Inc. holds 2 FDA 510(k) medical device clearances, cleared in 1978.

Top product codes for Cutler Laboratories, Inc.

DJC — Clinical Toxicology1 device
FPA — General Hospital1 device

Recent clearances by Cutler Laboratories, Inc.

K781785 — I.V. SET WITH IN-LINE FILTERCode FPA·1978-12-07
K781140 — CUTTER RESIFLEX FOLEY CATHETERSCode DJC·1978-09-07

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