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

PORTEX EMERGENCY CRICOTHYROIDOTOMY KIT

K Number: K050166 · Decision May 26, 2005
Classifications
1
FEI Numbers
14
Registration Numbers
14
Same Product Code
13
Applicant Total
3
Review Days
120

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Basic Information

Device Name
PORTEX EMERGENCY CRICOTHYROIDOTOMY KIT
K Number
K050166
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5090
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Smiths Medical
Date Received
January 26, 2005
Decision Date
May 26, 2005
Product Code
BWC
Advisory Committee
Anesthesiology
Review Advisory Committee
AN
Third Party
N

Classifications

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

Product Code Device Name
BWC Needle, Emergency Airway

Similar 510(k) Clearances

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Other Clearances by Smiths Medical

K Number Device Name
K181660 Acapella Choice Blue Vibratory PEP Device
K041348 PORTEX ULTRAPERC PERCUTANEOUS DILATION TRACHEOSTOMY KIT_WITH SERIAL DILATORS OR SINGLE STAGE DILATOR, BLUE LINE ULTRA