510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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PTLClass II

Wire, Guide, Catheter, Exempt

21 CFR 870.1330 / Cardiovascular
FDA source (opens on fda.gov)

PTL is the FDA product code for Wire, Guide, Catheter, Exempt, a class II device type, regulated under 21 CFR 870.1330. FDA's definition for this code reads: "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...". As of , FDA records hold no 510(k) clearances under this code and no recalls.

Classification record

Product code
PTL
Device name
Wire, Guide, Catheter, Exempt
FDA 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.
Regulation
21 CFR 870.1330
Device class
Class II
Review panel
Cardiovascular
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
0
Ingested recalls
0

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 29 companies shown, in name order