Heyer-Schulte Syringo Peritoneal Shunt

FDA 510(k) K854049 · American V. Mueller

Substantially Equivalent

510(k) numberK854049

Submission

Device name
Heyer-Schulte Syringo Peritoneal Shunt
Applicant
American V. Mueller
Chicago, IL, US
Received
October 3, 1985
Decision date
November 27, 1985
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
JXG – Shunt, Central Nervous System And Components
Device class
Class II (moderate risk)
Regulation
21 CFR 882.5550
Specialty
Neurology
Implant
Yes

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More from Aesculap, Inc.

510(k)DeviceDecision
K873771Heyer-Schulte(R) One Piece Shunt Vent. Cath. IntroGYK · Traditional 12/18/1987SE
K873332Maxivac(Tm) Closed Wound Suction Drainage SystemGCY · Traditional 09/08/1987SE
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
K851082V. Mueller Blom-Singer Esophageal Insufflation TesENW · Traditional 07/22/1985SE
K851974V. Mueller Vital Skin StaplerGDT · Traditional 06/11/1985SE
K850947V-Mueller Inverted Linear Anastomosis InstrumentsGAG · Traditional 04/17/1985SE

Questions and answers

When was Heyer-Schulte Syringo Peritoneal Shunt cleared by the FDA?

Heyer-Schulte Syringo Peritoneal Shunt (K854049) received a 510(k) decision of Substantially Equivalent on November 27, 1985, 55 days after the submission was received.

What is the product code of K854049?

The FDA product code is JXG – Shunt, Central Nervous System And Components, a Class II (moderate risk) device regulated under 21 CFR 882.5550.