Polyfin Extension Set, Models 126 and 128

FDA 510(k) K965208 · Medtronic Minimed

Substantially Equivalent

510(k) numberK965208

Submission

Device name
Polyfin Extension Set, Models 126 and 128
Applicant
Medtronic Minimed
Sylmar, CA, US
Received
December 27, 1996
Decision date
February 26, 1997
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
FPK – Tubing, Fluid Delivery
Device class
Class II (moderate risk)
Regulation
21 CFR 880.5440
Specialty
General Hospital

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Questions and answers

When was Polyfin Extension Set, Models 126 and 128 cleared by the FDA?

Polyfin Extension Set, Models 126 and 128 (K965208) received a 510(k) decision of Substantially Equivalent on February 26, 1997, 61 days after the submission was received.

What is the product code of K965208?

The FDA product code is FPK – Tubing, Fluid Delivery, a Class II (moderate risk) device regulated under 21 CFR 880.5440.