FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

CUFFED LINDER NASOTRACHEAL AIRWAY

K Number: K900457 · Decision Apr 16, 1990
Classifications
1
FEI Numbers
132
Registration Numbers
132
Same Product Code
240
Applicant Total
20
Review Days
76

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Basic Information

Device Name
CUFFED LINDER NASOTRACHEAL AIRWAY
K Number
K900457
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5730
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Polamedco, Inc.
Date Received
January 30, 1990
Decision Date
April 16, 1990
Product Code
BTR
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
BTR Tube, Tracheal (W/Wo Connector)

Similar 510(k) Clearances

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Other Clearances by Polamedco, Inc.

K Number Device Name
K983000 CRICOTHYROTOMY TUBE
K954383 SURELOC CIRCUIT CONNECTOR
K953793 INTROSCOPE
K950713 AIRGUIDE STYLETTE
K933596 GASTRIC, CATHETER, IRRIGATION & ASPIRATION
K950380 FLEXTITIP STYLETTE
K920900 POLAMEDCO TRACHEAL AND NASOTRACHEAL TUBES
K900456 POLAMEDCO NASOPAHARYNGEAL AIRWAY
K894516 VISOSHIELD(TM), SURGICAL EYE PROTECTOR
K881496 LINDER NASOTRACHEAL AIRWAY
Search all 20 clearances from Polamedco, Inc. →