← FDA Medical Device Classifications

Catheter, Peritoneal Dialysis, Single Use, Exempt

PTV · Class II — Moderate Risk (510(k) clearance required) · Gastroenterology, Urology · 21 CFR 876.5630

Classification

FDA Product Code
PTV
Device class
Class II — Moderate Risk (510(k) clearance required)
Regulation
21 CFR 876.5630
Review panel
GU
Medical specialty
Gastroenterology, Urology
Submission type
4
GMP exempt
N
Life sustaining
Y
Implant
N
Third-party review
N

Definition

This product code is the class II exempt counterpart of FKO, 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 876.9 and the specific limitations of exemption as stated in the “Physical State” field of this product code description.

Market data

Cleared 510(k) submissions
0
Registered establishments
0

Source

Authoritative
FDA Device Classification database
Machine
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