510(k) K810888

BOUNDARY TUBING HOLDERS by The Buckeye Cellulose Corp. — Product Code FZX

K810888 is an FDA 510(k) premarket notification submitted by The Buckeye Cellulose Corp. for the device "BOUNDARY TUBING HOLDERS". The FDA issued a decision of Substantially Equivalent on April 23, 1981. The device falls under product code FZX (Guide, Surgical, Instrument), a Class I device regulated under 21 CFR 878.4800. The Buckeye Cellulose Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 23, 1981
Date Received
April 2, 1981
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Guide, Surgical, Instrument
Device Class
Class I
Regulation Number
878.4800
Review Panel
SU
Submission Type