510(k) K850644

NASOPHARYNGEAL AIRWAY-ROBERTAZZI by Dryden Corp. — Product Code BTQ

K850644 is an FDA 510(k) premarket notification submitted by Dryden Corp. for the device "NASOPHARYNGEAL AIRWAY-ROBERTAZZI". The FDA issued a decision of Substantially Equivalent on March 21, 1985. The device falls under product code BTQ (Airway, Nasopharyngeal), a Class I device regulated under 21 CFR 868.5100. Dryden Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 21, 1985
Date Received
February 19, 1985
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