510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K864937Substantially Equivalent

'Exmoor' Zoellner Sucker Ends

Exmoor Plastics Limited, Taunton, GB / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K864937 is the FDA 510(k) clearance record for 'EXMOOR' ZOELLNER SUCKER ENDS, a class II device, cleared for Exmoor Plastics , Ltd. on under FDA product code JOL (Catheter And Tip, Suction). FDA records list 43 510(k) clearances for Exmoor Plastics , Ltd., from to . As of , FDA records show no recalls naming K864937.

Clearance record

Decision date
Received
(104 days to decision)
Product code
JOL Catheter And Tip, Suction
Regulation
21 CFR 880.6740
Device class
Class II
Review panel
General Hospital
Applicant
Exmoor Plastics , Ltd. Lisieux Way, Taunton, GB
Third party review
No

Clearances, product code JOL

Trailing 12 months

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

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