Circle Nephrostomy Tube Introducer

FDA 510(k) K810533 · American V. Mueller

Substantially Equivalent

510(k) numberK810533

Submission

Device name
Circle Nephrostomy Tube Introducer
Applicant
American V. Mueller
Mchenry, IL, US
Received
February 26, 1981
Decision date
March 11, 1981
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
KOA – Surgical Instruments, G-U, Manual (And Accessories)
Device class
Class I (low risk)
Regulation
21 CFR 876.4730
Specialty
Gastroenterology, Urology

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More from Annex Medical, Inc.

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K873771Heyer-Schulte(R) One Piece Shunt Vent. Cath. IntroGYK · Traditional 12/18/1987SE
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K871685Heyer-Schulte Spetzler Lumbar-Peritoneal Shunt SysJXG · Traditional 06/12/1987SE
K864676Heyer-Schulte Hermetic External CSF Drain. SystemJXG · Traditional 12/29/1986SE
K862772V. Mueller (R) Gooseneck Circular StaplerGAG · Traditional 08/18/1986SE
K861471V. Mueller Vital Clip-Hemostatic ClipFZP · Traditional 06/06/1986SE
K854568V. Mueller Pneumo-Intestinal 15 Vascular & 30 StapGEF · Traditional 12/02/1985SE
K854049Heyer-Schulte Syringo Peritoneal ShuntJXG · Traditional 11/27/1985SE
K851082V. Mueller Blom-Singer Esophageal Insufflation TesENW · Traditional 07/22/1985SE
K851974V. Mueller Vital Skin StaplerGDT · Traditional 06/11/1985SE

Questions and answers

When was Circle Nephrostomy Tube Introducer cleared by the FDA?

Circle Nephrostomy Tube Introducer (K810533) received a 510(k) decision of Substantially Equivalent on March 11, 1981, 13 days after the submission was received.

What is the product code of K810533?

The FDA product code is KOA – Surgical Instruments, G-U, Manual (And Accessories), a Class I (low risk) device regulated under 21 CFR 876.4730.