510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K854049Substantially Equivalent

Heyer-Schulte Syringo Peritoneal Shunt

American V. Mueller, Chicago IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K854049 is the FDA 510(k) clearance record for HEYER-SCHULTE SYRINGO PERITONEAL SHUNT, a class II device, cleared for American V. Mueller on under FDA product code JXG (Shunt, Central Nervous System And Components). FDA records list 31 510(k) clearances for American V. Mueller, from to . As of , FDA records show 5 recalls naming K854049.

Clearance record

Decision date
Received
(55 days to decision)
Product code
JXG Shunt, Central Nervous System And Components
Regulation
21 CFR 882.5550
Device class
Class II
Review panel
Neurology
Applicant
American V. Mueller 6600 W. Touhy, Chicago IL
Third party review
No

Clearances, product code JXG

Trailing 12 months
4 clearances under product code JXG in the twelve months to October 2026, November 2025 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code JXG, trailing twelve months
MonthClearances
November 20252
December 20251
January 20260
February 20260
March 20260
April 20260
May 20260
June 20261
July 20260
August 20260
September 20260
October 20260