FDA Data MCP
☰
Docs
Datasets
Pricing
Blog
Account
Statistics
Get API Key
Home
/
Companies
/ Incredivision, Inc.
Incredivision, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K940962
LIQUID LIGHT 500
April 8, 1994
K940963
XENON LIGHT SOURCE
April 8, 1994