510(k) K900456

POLAMEDCO NASOPAHARYNGEAL AIRWAY by Polamedco, Inc. — Product Code BTQ

K900456 is an FDA 510(k) premarket notification submitted by Polamedco, Inc. for the device "POLAMEDCO NASOPAHARYNGEAL AIRWAY". The FDA issued a decision of Substantially Equivalent on April 19, 1990. The device falls under product code BTQ (Airway, Nasopharyngeal), a Class I device regulated under 21 CFR 868.5100. Polamedco, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 19, 1990
Date Received
January 30, 1990
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Airway, Nasopharyngeal
Device Class
Class I
Regulation Number
868.5100
Review Panel
AN
Submission Type