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

LAPAROSCOPIC ELECTROSURGICAL CANNULA W/RETRACTABLE

K Number: K912637 · Decision Oct 4, 1991
Classifications
1
FEI Numbers
839
Registration Numbers
839
Same Product Code
2251
Applicant Total
38
Review Days
112

Basic Information

Device Name
LAPAROSCOPIC ELECTROSURGICAL CANNULA W/RETRACTABLE
K Number
K912637
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4400
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
DEXIDE, INC.
Date Received
June 14, 1991
Decision Date
October 4, 1991
Product Code
GEI
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
GEI Electrosurgical, Cutting & Coagulation & Accessories

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K981941 MULTAPORT CANNULA REDUCER AND ACCESSORIES
K953611 DEXIDE ENDO-LUBE KIT
K944509 DEXIDE INSUFFLATION TUBING WITH FILTER
K924117 DEXIDE LAPAROSCOPIC KITS
K923845 DEXIDE LAPAROSCOPIC ACCESSORIES
K921709 ENDOBAG, MODIFICATION
K913762 MONOSCOPY(TM) BRAND, ENDOBAG
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