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

SYMBIOSIS MONOPLAR ELECTROSURGICAL ELECTRODES

K Number: K953242 · Decision Oct 6, 1995
Classifications
1
FEI Numbers
54
Registration Numbers
54
Same Product Code
43
Applicant Total
34
Review Days
87

Basic Information

Device Name
SYMBIOSIS MONOPLAR ELECTROSURGICAL ELECTRODES
K Number
K953242
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.4160
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
SYMBIOSIS CORP.
Date Received
July 11, 1995
Decision Date
October 6, 1995
Product Code
KNF
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
KNF Coagulator-Cutter, Endoscopic, Unipolar (And Accessories)

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (KNF), ordered by most recent decision date.

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Other Clearances by SYMBIOSIS CORP.

K Number Device Name
K955119 SYMBIOSIS MONOPOLAR ELECTROSURGICAL ROLLER ELECTRODES
K953453 SYMBIOSIS MONOPOLAR ELECTROSURGICAL ROLLER ELECTRODES
K952432 SYMBIOSIS BIPOLAR FORCEPS
K951387 SYMBIOSIS BIPOLAR SCISSORS
K950286 SYMBIOSIS BIPOLAR SCISSORS
K946238 SYMBIOSIS GASTROINTESTINAL BIOPSY FORCEPS
K930773 SYMBIOSIS GYNECOLOGICAL BIOPSY FORCEPS
K941426 SYMBIOSIS REUSABLE MONOPOLAR ELECTROSURGICAL PROBE
K932266 SYMBIOSIS DISPOS GASTRO BIOPSY FORCEPS W/REUSE HAN
K931957 SYMBIOSIS DISPOSABLE UROLOGICAL BIOPSY FORCEPS
Search all 34 clearances from SYMBIOSIS CORP. →