510(k) K891401

HEMOSTATIC FORCEPS BRUNS.,GEMINI,SPENCER-WELL,KANT by Zinnanti Surgical Instruments, Inc. — Product Code GEN

K891401 is an FDA 510(k) premarket notification submitted by Zinnanti Surgical Instruments, Inc. for the device "HEMOSTATIC FORCEPS BRUNS.,GEMINI,SPENCER-WELL,KANT". The FDA issued a decision of Substantially Equivalent on April 6, 1989. The device falls under product code GEN (Forceps, General & Plastic Surgery), a Class I device regulated under 21 CFR 878.4800. Zinnanti Surgical Instruments, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 6, 1989
Date Received
March 14, 1989
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Forceps, General & Plastic Surgery
Device Class
Class I
Regulation Number
878.4800
Review Panel
SU
Submission Type