FDA 510(k) FDA class 2 Substantially Equivalent 🇬🇧 United Kingdom

'EXMOOR' ZOELLNER SUCKER ENDS

K Number: K864937 · Decision Mar 30, 1987
Classifications
1
FEI Numbers
331
Registration Numbers
331
Same Product Code
83
Applicant Total
43
Review Days
104

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Basic Information

Device Name
'EXMOOR' ZOELLNER SUCKER ENDS
K Number
K864937
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.6740
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Exmoor Plastics , Ltd.
Date Received
December 16, 1986
Decision Date
March 30, 1987
Product Code
JOL
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
JOL Catheter And Tip, Suction

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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. →