14F X 55CM Ash Split-Cath XL, Model ASPC55-XL

FDA 510(k) K020315 · Medcomp

Unknown

510(k) numberK020315

Submission

Device name
14F X 55CM Ash Split-Cath XL, Model ASPC55-XL
Applicant
Medcomp
Harleysville, PA, US
Received
January 29, 2002
Decision date
May 24, 2002
Decision
Unknown (SESK)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
MSD – Catheter, Hemodialysis, Implanted
Device class
Class II (moderate risk)
Regulation
21 CFR 876.5540
Specialty
Gastroenterology, Urology
Implant
Yes
Life-sustaining
Yes

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Questions and answers

When was 14F X 55CM Ash Split-Cath XL, Model ASPC55-XL cleared by the FDA?

14F X 55CM Ash Split-Cath XL, Model ASPC55-XL (K020315) received a 510(k) decision of Unknown on May 24, 2002, 115 days after the submission was received.

What is the product code of K020315?

The FDA product code is MSD – Catheter, Hemodialysis, Implanted, a Class II (moderate risk) device regulated under 21 CFR 876.5540.