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

LASER RECTOSCOPE SET 784

K Number: K842997 · Decision Aug 27, 1984
Classifications
1
FEI Numbers
38
Registration Numbers
38
Same Product Code
10
Applicant Total
20
Review Days
28

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Basic Information

Device Name
LASER RECTOSCOPE SET 784
K Number
K842997
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Laser Industries , Ltd.
Date Received
July 30, 1984
Decision Date
August 27, 1984
Product Code
FDC
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
FDC Resectoscope, Working Element

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