510(K) CLEARANCES 49 ▼18RECALLS POSTED 23 ▼3CLASS I 1 ▼1PMA DECISIONS 37 ▼3WEEK ENDING / FDA DATA AS OF
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K873852Substantially Equivalent

Infusion Manifold

Advanced Surgical Products, Inc., Chesterfield MO / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K873852 is the FDA 510(k) clearance record for INFUSION MANIFOLD, a class II device, cleared for Advanced Surgical Products, Inc. on under FDA product code FPK (Tubing, Fluid Delivery). FDA records list 64 510(k) clearances for Advanced Surgical Products, Inc., from to . As of , FDA records show no recalls naming K873852.

Clearance record

Decision date
Received
(62 days to decision)
Product code
FPK Tubing, Fluid Delivery
Regulation
21 CFR 880.5440
Device class
Class II
Review panel
General Hospital
Applicant
Advanced Surgical Products, Inc. 744 Goddard, Chesterfield MO
Third party review
No

Clearances, product code FPK

Trailing 12 months

FDA records hold no clearances under product code FPK in the trailing twelve months.

FDA records show no clearances under product code FPK in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code FPK, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260