510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K854593Substantially Equivalent

Norfolk Medical Peritoneal-Access Port

Norfolk Medical Products, Inc., Skokie IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K854593 is the FDA 510(k) clearance record for NORFOLK MEDICAL PERITONEAL-ACCESS PORT, a class III device, cleared for Norfolk Medical Products, Inc. on under FDA product code LMQ (Device, Peritoneal Access, Subcutaneous, Implanted). FDA records list 20 510(k) clearances for Norfolk Medical Products, Inc., from to . As of , FDA records show no recalls naming K854593.

Clearance record

Decision date
Received
(78 days to decision)
Product code
LMQ Device, Peritoneal Access, Subcutaneous, Implanted
Device class
Class III
Review panel
Unknown
Applicant
Norfolk Medical Products, Inc. 7307 N. Ridgeway, Skokie IL
Third party review
No

Clearances, product code LMQ

Trailing 12 months

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

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