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

ENDOSCOPIC ANTI FOG DEVICE

K Number: K993604 · Decision Mar 3, 2000
Classifications
1
FEI Numbers
64
Registration Numbers
64
Same Product Code
26
Applicant Total
9
Review Days
130

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Basic Information

Device Name
ENDOSCOPIC ANTI FOG DEVICE
K Number
K993604
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Mectra Labs, Inc.
Date Received
October 25, 1999
Decision Date
March 3, 2000
Product Code
OCT
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
OCT Anti Fog Solution And Accessories, Endoscopy

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