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

PRESCOTT'S LIGHT SOURCE MODEL NO. II-150

K Number: K964586 · Decision Jan 17, 1997
Classifications
1
FEI Numbers
59
Registration Numbers
59
Same Product Code
30
Applicant Total
1
Review Days
63

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Basic Information

Device Name
PRESCOTT'S LIGHT SOURCE MODEL NO. II-150
K Number
K964586
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Iba/Griffith
Date Received
November 15, 1996
Decision Date
January 17, 1997
Product Code
FCW
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
FCW Light Source, Fiberoptic, Routine

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