510(k) K853367

H-H BURR HOLE CATHETER SUPPORT by Holter-Hausner Intl. — Product Code GXR

K853367 is an FDA 510(k) premarket notification submitted by Holter-Hausner Intl. for the device "H-H BURR HOLE CATHETER SUPPORT". The FDA issued a decision of Substantially Equivalent on September 11, 1985. The device falls under product code GXR (Cover, Burr Hole), a Class II device regulated under 21 CFR 882.5250. Holter-Hausner Intl. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 11, 1985
Date Received
August 21, 1985
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Cover, Burr Hole
Device Class
Class II
Regulation Number
882.5250
Review Panel
NE
Submission Type