510(k) K840314

CAT 10-NEUROLOGY DEVICE by Imm Enterprises , Ltd. — Product Code GWZ

K840314 is an FDA 510(k) premarket notification submitted by Imm Enterprises , Ltd. for the device "CAT 10-NEUROLOGY DEVICE". The FDA issued a decision of Substantially Equivalent on February 23, 1984. The device falls under product code GWZ (Percussor), a Class I device regulated under 21 CFR 882.1700. Imm Enterprises , Ltd. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 23, 1984
Date Received
January 24, 1984
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Percussor
Device Class
Class I
Regulation Number
882.1700
Review Panel
NE
Submission Type