FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

EXMOOR AURAL GROMMET AG/T3

K Number: K810704 · Decision Apr 14, 1981
Classifications
1
FEI Numbers
33
Registration Numbers
33
Same Product Code
114
Applicant Total
43
Review Days
29

Basic Information

Device Name
EXMOOR AURAL GROMMET AG/T3
K Number
K810704
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
874.3880
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Applicant
EXMOOR PLASTICS LTD.
Date Received
March 16, 1981
Decision Date
April 14, 1981
Product Code
ETD
Advisory Committee
Ear, Nose, Throat
Review Advisory Committee
EN
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
ETD Tube, Tympanostomy

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Other Clearances by EXMOOR PLASTICS LTD.

K Number Device Name
K093863 EPIDRUM
K990366 EXMOOR SUCTION CLEARANCE KIT
K980828 EXMOOR MYRINGOTOMY KIT
K981143 DILKES LASER/SUCTION CANNULAE
K972700 EXMOOR ATTIC AND MASTOID ANTRUM MIDDLE EAR IMPLANT (EMMETT CAMPBELL MD FACS PATTERN)
K981088 MILLS COLUMELLA PROSTHESIS
K981045 EXMOOR TEFLON LOOP REPLACEMENT PROSTHESIS
K974008 PFLEIDERER'S INTRATYMPANIC CATHETER
K974224 ENDOLYMPHATIC SAC TO MASTOID T-SHUNT
K973587 EXMOOR TYMPANOCENTESIS KIT (TK/1)
Search all 43 clearances from EXMOOR PLASTICS LTD. →