510(k) K896263

RHINOMANOMETER by Jedmed Instrument Co. — Product Code BXQ

K896263 is an FDA 510(k) premarket notification submitted by Jedmed Instrument Co. for the device "RHINOMANOMETER". The FDA issued a decision of Substantially Equivalent on April 16, 1990. The device falls under product code BXQ (Rhinoanemometer (Measurement Of Nasal Decongestion)), a Class II device regulated under 21 CFR 868.1800. Jedmed Instrument Co. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 16, 1990
Date Received
October 31, 1989
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Rhinoanemometer (Measurement Of Nasal Decongestion)
Device Class
Class II
Regulation Number
868.1800
Review Panel
AN
Submission Type