FDA Data MCP
☰
Docs
Datasets
Pricing
Blog
Account
Statistics
Get API Key
Home
/
Companies
/ Robert R. Moore
Robert R. Moore
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
5
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K770658
EXERCISER, LEG, LOWER EXTREMITY
June 17, 1977
K770501
KNEE CUFF FOR EXPRESSING FLUID
April 5, 1977
K770223
HEAVY FOAM HEEL & ELBOW PROTECTORS
February 23, 1977
K770060
X-RAY POSITIONING DEVICE
January 24, 1977
K770059
ORTHOPEDIC SPECIALTIES
January 14, 1977