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

DEXIDE INSUFFLATION TUBING WITH FILTER

K Number: K944509 · Decision Feb 7, 1995
Classifications
1
FEI Numbers
141
Registration Numbers
141
Same Product Code
176
Applicant Total
38
Review Days
145

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Basic Information

Device Name
DEXIDE INSUFFLATION TUBING WITH FILTER
K Number
K944509
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.1730
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Dexide, Inc.
Date Received
September 15, 1994
Decision Date
February 7, 1995
Product Code
HIF
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
HIF Insufflator, Laparoscopic

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Other Clearances by Dexide, Inc.

K Number Device Name
K991814 MULTACHOICE INSTRUMENTS
K990379 MODIFICATION TO MULTAPORT CANNULA, REDUCER AND ACCESSORIES
K981940 MULTAPUMP DISPOSABLE PUMP HEAD AND ACCESSORIES
K981941 MULTAPORT CANNULA REDUCER AND ACCESSORIES
K953611 DEXIDE ENDO-LUBE KIT
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. →