510(k) K896298

JEDMED S CHAIR by Jedmed Instrument Co. — Product Code ETF

K896298 is an FDA 510(k) premarket notification submitted by Jedmed Instrument Co. for the device "JEDMED S CHAIR". The FDA issued a decision of Substantially Equivalent on January 26, 1990. The device falls under product code ETF (Unit, Examining/Treatment, Ent), a Class I device regulated under 21 CFR 874.5300. Jedmed Instrument Co. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 26, 1990
Date Received
October 30, 1989
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Unit, Examining/Treatment, Ent
Device Class
Class I
Regulation Number
874.5300
Review Panel
EN
Submission Type