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/ N.M. Beale Co., Inc.
N.M. Beale Co., Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
5
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K093584
EZ-MISTER
March 4, 2011
K093329
SCOPE INTRODUCER MODEL 7400
February 16, 2010
K071579
PEF TUBE
November 20, 2007
K992178
BALLOON FOR ULTRASONIC ENDOSCOPES
May 12, 2000
K903834
N. M. BEALE COMPANY VU-THRU WATER BOTTLE
September 24, 1990