Company · US

Medcraft Corp.

FDA 510(k) clearances and medical device recalls filed under this name, 1976 to 1986. 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
DPS	Electrocardiograph	2
DSH	Recorder, Magnetic Tape, Medical	1
IOL	Treadmill, Powered	1
QGH	Electroconvulsive Therapy Device For Catatonia, Major Depressive Disorder, And Bipolar Disorder	1

Decided	510(k)	Device and applicant	Code
Nov 10, 1986	K860467	ELECTROSHOCK UNIT NEUROLOGY MODEL B-25 Medcraft Corp.	QGH
Sep 27, 1979	K791795	COMP-ACT IV Medcraft Corp.	DPS
Aug 30, 1976	K760510	MONITORING SYSTEM, REHABILITATION Medcraft Corp.	DPS
Aug 30, 1976	K760509	TREADMILL, DIAGNOSTIC Medcraft Corp.	IOL
Aug 30, 1976	K760508	ACCUTAPE 24 Medcraft Corp.	DSH

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