EXMOOR TYMPANOCENTESIS KIT (TK/1)— 510(k) K973587

Name: FDA 510(k) clearance K973587
Creator: U.S. Food and Drug Administration
Published: 1998-01-23

Substantially Equivalent

Exmoor Plastics , Ltd.

FDA 510(k) clearance K973587 for EXMOOR TYMPANOCENTESIS KIT (TK/1), Substantially Equivalent on 1998-01-23. Applicant: Exmoor Plastics , Ltd.. Device class: 1.

Clearance details

Applicant: Exmoor Plastics , Ltd.
Product code: Code JZF
Device class: Class 1
Regulation: 21 CFR 874.4420
Advisory panel: Ear, Nose, Throat
Date received: 1997-09-22
Decision date: 1998-01-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Taunton, GB

Download summary PDF View on FDA.gov ↗

Recent devices under product code JZF

view all

K862903 — MIDDLE EAR VIEWER AND FLUID COLLECTOR1986-11-24
K853589 — SHAH SELF-CLEARING MASTOID SUCTION TUBE1985-12-23
K841357 — MICRO FLUID APPLICATOR1984-08-24
K822010 — RIGID SUCTION TIPS & RELATED ITEMS1982-08-12

More clearances from Exmoor Plastics , Ltd.

view all

K093863 — EPIDRUM2010-05-10
K990366 — EXMOOR SUCTION CLEARANCE KIT1999-03-05
K980828 — EXMOOR MYRINGOTOMY KIT1998-10-22
K981143 — DILKES LASER/SUCTION CANNULAE1998-09-14
K972700 — EXMOOR ATTIC AND MASTOID ANTRUM MIDDLE EAR IMPLANT (EMMETT CAMPBELL MD FACS PATTERN)1998-07-16

Data sourced from openFDA. This site is unofficial and independent of the FDA.