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

SHILEY LARYNGECTOMY TUBE

K Number: K821993 · Decision Aug 12, 1982
Classifications
1
FEI Numbers
35
Registration Numbers
35
Same Product Code
3
Applicant Total
174
Review Days
36

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Basic Information

Device Name
SHILEY LARYNGECTOMY TUBE
K Number
K821993
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
874.4420
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Applicant
Shiley, Inc.
Date Received
July 7, 1982
Decision Date
August 12, 1982
Product Code
KAC
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
KAC Tube, Laryngectomy

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K911876 SHILEY PLEXUS(R) VENOUS RESERVOIR, PVR1200
K910923 BCD ADVANCED
K901548 BIOMEDICAL SENSORS-SHILEY BGM 4000 INTRA BLOOD GAS
K903435 SHILEY SPECIALIZED TRACHEOSTOMY TUBE
K901624 SHILEY PLEXUS INTEGRAL RESERVOIR HOLLOW FIBER OXY.
K901250 PLEXUS 2(TM) INFANT HOLLOW FIBER OXYGENATOR
K901249 PLEXUS 3.5(TM) PEDIATRIC HOLLOW FIBER OXYGENATOR
K900797 STOCKERT SHILEY DUAL PRESSURE CONTROL MODULE XR
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