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

LINDER NASOPHARYNGEAL AIRWAY

K Number: K843524 · Decision Oct 4, 1984
Classifications
1
FEI Numbers
122
Registration Numbers
122
Same Product Code
18
Applicant Total
20
Review Days
28

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Basic Information

Device Name
LINDER NASOPHARYNGEAL AIRWAY
K Number
K843524
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
868.5100
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Polamedco, Inc.
Date Received
September 6, 1984
Decision Date
October 4, 1984
Product Code
BTQ
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
BTQ Airway, Nasopharyngeal

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
K900457 CUFFED LINDER NASOTRACHEAL AIRWAY
K894516 VISOSHIELD(TM), SURGICAL EYE PROTECTOR
Search all 20 clearances from Polamedco, Inc. →