510(k) K891034

TISCHLER BIOPSY FORCEPS by Zinnanti Surgical Instruments, Inc. — Product Code HFB

K891034 is an FDA 510(k) premarket notification submitted by Zinnanti Surgical Instruments, Inc. for the device "TISCHLER BIOPSY FORCEPS". The FDA issued a decision of Substantially Equivalent on March 17, 1989. The device falls under product code HFB (Forceps, Biopsy, Gynecological), a Class I device regulated under 21 CFR 884.4530. Zinnanti Surgical Instruments, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 17, 1989
Date Received
February 28, 1989
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Forceps, Biopsy, Gynecological
Device Class
Class I
Regulation Number
884.4530
Review Panel
OB
Submission Type