510(k) K896263
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