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

MODIFICATION TO MULTAPORT CANNULA, REDUCER AND ACCESSORIES

K Number: K990379 · Decision Mar 4, 1999
Classifications
1
FEI Numbers
548
Registration Numbers
548
Same Product Code
1422
Applicant Total
38
Review Days
24

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Basic Information

Device Name
MODIFICATION TO MULTAPORT CANNULA, REDUCER AND ACCESSORIES
K Number
K990379
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Dexide, Inc.
Date Received
February 8, 1999
Decision Date
March 4, 1999
Product Code
GCJ
Advisory Committee
Gastroenterology, Urology
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
GCJ Laparoscope, General & Plastic Surgery

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Other Clearances by Dexide, Inc.

K Number Device Name
K991814 MULTACHOICE INSTRUMENTS
K981940 MULTAPUMP DISPOSABLE PUMP HEAD AND ACCESSORIES
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
K912637 LAPAROSCOPIC ELECTROSURGICAL CANNULA W/RETRACTABLE
Search all 38 clearances from Dexide, Inc. →