510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K962814Substantially Equivalent

Denver Pleural Effusion Shunt with External Pump Chamber

Denver Biomaterials, Inc., Evergreen CO / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K962814 is the FDA 510(k) clearance record for DENVER PLEURAL EFFUSION SHUNT WITH EXTERNAL PUMP CHAMBER, a class II device, cleared for Denver Biomaterials, Inc. on under FDA product code KPM (Shunt, Peritoneal). FDA records list 4 510(k) clearances for Denver Biomaterials, Inc., from to . As of , FDA records show no recalls naming K962814.

Clearance record

Decision date
Received
(269 days to decision)
Product code
KPM Shunt, Peritoneal
Regulation
21 CFR 876.5955
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Denver Biomaterials, Inc. 6851 Hwy. 73, Evergreen CO
510(k) summary
Summary
Third party review
No

Clearances, product code KPM

Trailing 12 months

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

FDA records show no clearances under product code KPM in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code KPM, 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