Company · US

N.M. Beale Co., Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1990 to 2011. Name variants (Inc, Corp, punctuation) are merged.

5510(k) clearances (0 in 12 months)

0recalls (0 in 12 months)

0recalls that name a 510(k)

Product codes

Code	Device	Records
CCT	Applicator (Laryngo-Tracheal), Topical Anesthesia	1
ITX	Transducer, Ultrasonic, Diagnostic	1
KNT	Tubes, Gastrointestinal (And Accessories)	1
OCX	Endoscopic Irrigation/Suction System	1
ODC	Endoscope Channel Accessory	1

Decided	510(k)	Device and applicant	Code
Mar 4, 2011	K093584	EZ-MISTER N.M. Beale Co., Inc.	CCT
Feb 16, 2010	K093329	SCOPE INTRODUCER MODEL 7400 N.M. Beale Co., Inc.	ODC
Nov 20, 2007	K071579	PEF TUBE N.M. Beale Co., Inc.	KNT
May 12, 2000	K992178	BALLOON FOR ULTRASONIC ENDOSCOPES N.M. Beale Co., Inc.	ITX
Sep 24, 1990	K903834	N. M. BEALE COMPANY VU-THRU WATER BOTTLE N.M. Beale Co., Inc.	OCX

Date	Firm and product	Code	Linked 510(k)
No recalls in this window.