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

40LPM ABDOMINAL INSUFFLATOR, CATALOG # 72-00203-0

K Number: K022052 · Decision Jan 24, 2003
Classifications
1
FEI Numbers
141
Registration Numbers
141
Same Product Code
176
Applicant Total
55
Review Days
214

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Basic Information

Device Name
40LPM ABDOMINAL INSUFFLATOR, CATALOG # 72-00203-0
K Number
K022052
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.1730
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Northgate Technologies, Inc.
Date Received
June 24, 2002
Decision Date
January 24, 2003
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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