510(k) K931608

NCA-200 by Ics Medical Corp. — Product Code KHH

K931608 is an FDA 510(k) premarket notification submitted by Ics Medical Corp. for the device "NCA-200". The FDA issued a decision of Substantially Equivalent on June 22, 1993. The device falls under product code KHH (Stimulator, Caloric-Air), a Class I device regulated under 21 CFR 874.1800. Ics Medical Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 22, 1993
Date Received
April 1, 1993
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Stimulator, Caloric-Air
Device Class
Class I
Regulation Number
874.1800
Review Panel
EN
Submission Type