510(k) K910243

MOBILE TREATMENT CART by Jedmed Instrument Co. — Product Code ETF

K910243 is an FDA 510(k) premarket notification submitted by Jedmed Instrument Co. for the device "MOBILE TREATMENT CART". The FDA issued a decision of Substantially Equivalent on April 17, 1991. 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
April 17, 1991
Date Received
January 22, 1991
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