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

INSUFFLATOR FILTER TUBING SET

K Number: K945970 · Decision Dec 15, 1994
Classifications
1
FEI Numbers
33
Registration Numbers
33
Same Product Code
23
Applicant Total
4
Review Days
7

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Basic Information

Device Name
INSUFFLATOR FILTER TUBING SET
K Number
K945970
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Xylog Corp.
Date Received
December 8, 1994
Decision Date
December 15, 1994
Product Code
FCX
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

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

Product Code Device Name
FCX Insufflator, Automatic Carbon-Dioxide For Endoscope

Similar 510(k) Clearances

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

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Other Clearances by Xylog Corp.

K Number Device Name
K882048 MEDITRON ENDOLAV MODEL EL-100
K882049 MEDITRON MG-1000 MONOPOLAR GENERATOR
K874798 MEDITRON BI-2000 BIPOLAR GENERATOR W/IRRIGATION