510(k) K892549

SUCTION TUBES: HOUSE, BARON by Zinnanti Surgical Instruments, Inc. — Product Code GCX

K892549 is an FDA 510(k) premarket notification submitted by Zinnanti Surgical Instruments, Inc. for the device "SUCTION TUBES: HOUSE, BARON". The FDA issued a decision of Substantially Equivalent on May 18, 1989. The device falls under product code GCX (Apparatus, Suction, Operating-Room, Wall Vacuum Powered), a Class II device regulated under 21 CFR 880.6740. Zinnanti Surgical Instruments, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 18, 1989
Date Received
April 11, 1989
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Apparatus, Suction, Operating-Room, Wall Vacuum Powered
Device Class
Class II
Regulation Number
880.6740
Review Panel
HO
Submission Type