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Company · CA

Tenet Medical Engineering

FDA 510(k) clearances and medical device recalls filed under this name, 1996 to 1997. Name variants (Inc, Corp, punctuation) are merged.

3510(k) clearances (0 in 12 months)

3recalls (0 in 12 months)

0recalls that name a 510(k)

Product codes

Code	Device	Records
JEB	Table, Surgical With Orthopedic Accessories, Manual	3
FQO	Table, Operating-Room, Ac-Powered	1
GBB	Chair, Surgical, Ac-Powered	1
HHP	Table, Obstetrical, Manual (And Accessories)	1

Latest 510(k) clearances

Decided	510(k)	Device and applicant	Code
Feb 14, 1997	K963505	TENET MLTI-POSITIONING SURGICAL STIRRUP SYSTEM Tenet Medical Engineering, CA	HHP
Jan 9, 1997	K963506	TENET RADIOLUCENT HAND TABLE Tenet Medical Engineering, CA	FQO
Dec 5, 1996	K964102	TENET TIBIAL FRACTURE SUPPORT Tenet Medical Engineering, CA	GBB

Latest recalls

Date	Firm and product	Code	Linked 510(k)
Feb 26, 2008	Tenet Medical Engineering Inc TENET Medical Engineering Wrist Stabilization Kit, Large; REF (Part) #7693; Sterile; manufactured by TENET Medical Engineering, Calgary, Alberta, Canada T2Z 4M3. Terminated	JEB	None listed
Feb 26, 2008	Tenet Medical Engineering Inc TENET Medical Engineering Wrist Stabilization Kit, Medium; REF (Part) #7692; Sterile; manufactured by TENET Medical Engineering, Calgary, Alberta, Canada T2Z 4M3. Terminated	JEB	None listed
Feb 26, 2008	Tenet Medical Engineering Inc TENET Medical Engineering Wrist Stabilization Kit, Small; REF (Part) #7691; Sterile; manufactured by TENET Medical Engineering, Calgary, Alberta, Canada T2Z 4M3. Terminated	JEB	None listed

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