510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K973587Substantially Equivalent

Exmoor Tympanocentesis Kit (Tk/1)

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

K973587 is the FDA 510(k) clearance record for EXMOOR TYMPANOCENTESIS KIT (TK/1), a class I device, cleared for Exmoor Plastics , Ltd. on under FDA product code JZF (Tube, Ear Suction). FDA records list 43 510(k) clearances for Exmoor Plastics , Ltd., from to . As of , FDA records show no recalls naming K973587.

Clearance record

Decision date
Received
(123 days to decision)
Product code
JZF Tube, Ear Suction
Regulation
21 CFR 874.4420
Device class
Class I
Review panel
Ear, Nose, Throat
Applicant
Exmoor Plastics , Ltd. Lisieux Way, Taunton, GB
510(k) summary
Summary
Third party review
No

Clearances, product code JZF

Trailing 12 months

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

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