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

INSUFFLATION NEEDLE

K Number: K963359 · Decision Sep 24, 1996
Classifications
1
FEI Numbers
153
Registration Numbers
153
Same Product Code
336
Applicant Total
56
Review Days
29

Basic Information

Device Name
INSUFFLATION NEEDLE
K Number
K963359
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.1720
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
APPLIED MEDICAL RESOURCES
Date Received
August 26, 1996
Decision Date
September 24, 1996
Product Code
HET
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
HET Laparoscope, Gynecologic (And Accessories)

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