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

AIRGUIDE STYLETTE

K Number: K950713 · Decision May 17, 1995
Classifications
1
FEI Numbers
132
Registration Numbers
132
Same Product Code
31
Applicant Total
20
Review Days
91

Basic Information

Device Name
AIRGUIDE STYLETTE
K Number
K950713
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
868.5790
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
POLAMEDCO, INC.
Date Received
February 15, 1995
Decision Date
May 17, 1995
Product Code
BSR
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
BSR Stylet, Tracheal Tube

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K950380 FLEXTITIP STYLETTE
K920900 POLAMEDCO TRACHEAL AND NASOTRACHEAL TUBES
K900456 POLAMEDCO NASOPAHARYNGEAL AIRWAY
K900457 CUFFED LINDER NASOTRACHEAL AIRWAY
K894516 VISOSHIELD(TM), SURGICAL EYE PROTECTOR
K881496 LINDER NASOTRACHEAL AIRWAY
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