Kangaroo Entristar Skin-Level Gastrostomy Kit

FDA 510(k) K954429 · Sherwood Medical Co.

Unknown

510(k) numberK954429

Submission

Device name
Kangaroo Entristar Skin-Level Gastrostomy Kit
Applicant
Sherwood Medical Co.
St. Louis, MO, US
Received
September 22, 1995
Decision date
March 8, 1996
Decision
Unknown (SESK)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
KNT – Tubes, Gastrointestinal (And Accessories)
Device class
Class II (moderate risk)
Regulation
21 CFR 876.5980
Specialty
Gastroenterology, Urology

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Questions and answers

When was Kangaroo Entristar Skin-Level Gastrostomy Kit cleared by the FDA?

Kangaroo Entristar Skin-Level Gastrostomy Kit (K954429) received a 510(k) decision of Unknown on March 8, 1996, 168 days after the submission was received.

What is the product code of K954429?

The FDA product code is KNT – Tubes, Gastrointestinal (And Accessories), a Class II (moderate risk) device regulated under 21 CFR 876.5980.