FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

STI TISSUE MANIPULATOR

K Number: K911699 · Decision Jun 13, 1991
Classifications
1
FEI Numbers
28
Registration Numbers
28
Same Product Code
15
Applicant Total
28
Review Days
58

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Basic Information

Device Name
STI TISSUE MANIPULATOR
K Number
K911699
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.4150
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Applicant
Surgical Technologies, Inc.
Date Received
April 16, 1991
Decision Date
June 13, 1991
Product Code
HIN
Advisory Committee
Obstetrics/Gynecology
Review Advisory Committee
OB
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
HIN Coagulator-Cutter, Endoscopic, Bipolar (And Accessories)

Similar 510(k) Clearances

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Other Clearances by Surgical Technologies, Inc.

K Number Device Name
K941992 CYSTOSCOPE
K942029 ARTHROSCOPE
K946136 INFINITECH LIGHTED INFUSION CANNULA
K952566 OSCILFLATOR
K951918 SURGICAL TECHNOLOGIES, INC. SYRINGE
K950683 ARTHROGRAM TRAY
K946135 INFINITECH ASPIRATING LASER PROBE
K946181 INFINITECH SOFT TIP FLUTE NEEDLE
K942030 BIOPSY SCISSORS
K942482 PRESSURE MONITORING EXTENSION
Search all 28 clearances from Surgical Technologies, Inc. →