PTL — Wire, Guide, Catheter, Exempt Class II

FDA Device Classification

FDA product code PTL covers "Wire, Guide, Catheter, Exempt", a Class II medical device regulated under 21 CFR 870.1330. Submissions are reviewed by the Cardiovascular panel.

Classification Details

Product Code
PTL
Device Class
Class II
Regulation Number
870.1330
Submission Type
Review Panel
CV
Medical Specialty
Cardiovascular
Implant
No

Definition

This product code is the class II exempt counterpart of DQX, and was exempted, subject to the limitations of exemption, under the procedures established by the 21st Century Cures Act. This device type does not require premarket notification (510(k)) to market if it does not exceed the general limitations of exemption found in 21 CFR 870.9 and the specific limitations of exemption as stated in the “Physical State” field of this product code description.