#ES-32 Suction Catheter 32 Fr.

FDA 510(k) K970890 · Tri-Med Specialties, Inc.

Substantially Equivalent

510(k) numberK970890

Submission

Device name
#ES-32 Suction Catheter 32 Fr.
Applicant
Tri-Med Specialties, Inc.
Lenexa, KS, US
Received
March 11, 1997
Decision date
May 23, 1997
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement 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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K950574Needle/CannulaLRO · Traditional 02/24/1995SEKD
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K945160Paracentesis Needles/CannulasLRO · Traditional 11/14/1994SE
K924549Tri-Med Quick-Step(Tm) Rectal TubeGBT · Traditional 02/10/1994SE
K932015Tri-Med Inflatable Esophageal DilatorKNQ · Traditional 02/03/1994SE
K932652Tri-Med Paracentesis TrayLRO · Traditional 11/24/1993SEKD
K931201Tri-Med Endoscopic Fluid Introduction CatheterOCX · Traditional 09/28/1993SE

Questions and answers

When was #ES-32 Suction Catheter 32 Fr. cleared by the FDA?

#ES-32 Suction Catheter 32 Fr. (K970890) received a 510(k) decision of Substantially Equivalent on May 23, 1997, 73 days after the submission was received.

What is the product code of K970890?

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