510(k) K811440

EXP 600 PARALLEL PLATE DIALYZER by Extracorporeal Medical Specialities, Inc. — Product Code FJG

K811440 is an FDA 510(k) premarket notification submitted by Extracorporeal Medical Specialities, Inc. for the device "EXP 600 PARALLEL PLATE DIALYZER". The FDA issued a decision of Substantially Equivalent on Jun 12, 1981. The device falls under product code FJG (Dialyzer, Parallel Flow), a Class II device regulated under 21 CFR 876.5820. Extracorporeal Medical Specialities, Inc. has 68 other 510(k) clearances on record.

Clearance details

Decision
SESE (Substantially Equivalent)
Decision Date
Jun 12, 1981
Date Received
May 22, 1981
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device classification

Device Name
Dialyzer, Parallel Flow
Device Class
Class II
Regulation Number
876.5820
Review Panel
GU
Submission Type
510(k)

Source: FDA 510(k) database entry for K811440. Report a data issue: hello@regdatalab.com.