510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K874063Unknown

Enteron Abdominal Paracentesis Tray

Endovations, Camp Hill PA / Traditional, Unknown
FDA source (opens on fda.gov)

K874063 is the FDA 510(k) clearance record for ENTERON ABDOMINAL PARACENTESIS TRAY, a class I device, cleared for Endovations on under FDA product code KDD (Kit, Surgical Instrument, Disposable). FDA records list 38 510(k) clearances for Endovations, from to . As of , FDA records show 3 recalls naming K874063.

Clearance record

Decision date
Received
(60 days to decision)
Product code
KDD Kit, Surgical Instrument, Disposable
Regulation
21 CFR 878.4800
Device class
Class I
Review panel
General, Plastic Surgery
Applicant
Endovations 895 Poplar Church Rd., Camp Hill PA
Third party review
No

Clearances, product code KDD

Trailing 12 months

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

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