FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

THORACIC CATHETER (CHEST DRAINAGE TUBE)

K Number: K863142 · Decision Aug 29, 1986
Classifications
1
FEI Numbers
40
Registration Numbers
40
Same Product Code
26
Applicant Total
39
Review Days
14

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Basic Information

Device Name
THORACIC CATHETER (CHEST DRAINAGE TUBE)
K Number
K863142
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4200
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Sheridan Catheter Corp.
Date Received
August 15, 1986
Decision Date
August 29, 1986
Product Code
GBS
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
GBS Catheter, Ventricular, General & Plastic Surgery

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (GBS), ordered by most recent decision date.

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Other Clearances by Sheridan Catheter Corp.

K Number Device Name
K922894 LAZER-TRACH TRACHEAL TUBE
K897046 LASER RESISTANT TRACHEAL TUBE
K890823 ACCESSORY TO CLINICAL ELECTRONIC THERMOMETER
K884765 CLINICAL ELECTRONIC THERMOMETERS
K882918 KIM NASO-INTESTINAL TUBE
K882127 CLINICAL ELECTRONIC THERMOMETERS
K881368 CLINICAL ELECTONIC THERMOMETERS
K881293 SHERIDAN ELECTROSURGERY PROTECTION FILTER
K881873 INTRODUCTION/DRAINAGE CATHETER & ACCESS
K880960 NDYAG LASER TRACHEAL TUBE
Search all 39 clearances from Sheridan Catheter Corp. →