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

MARTIN COLD LIGHT FOUNTAIN

K Number: K932060 · Decision Mar 30, 1994
Classifications
1
FEI Numbers
548
Registration Numbers
548
Same Product Code
1422
Applicant Total
11
Review Days
335

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Basic Information

Device Name
MARTIN COLD LIGHT FOUNTAIN
K Number
K932060
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Medline
Date Received
April 29, 1993
Decision Date
March 30, 1994
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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