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Company · US

L H M Ent., Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1988 to 1990. Name variants (Inc, Corp, punctuation) are merged.

6510(k) clearances (0 in 12 months)

0recalls (0 in 12 months)

0recalls that name a 510(k)

Product codes

Code	Device	Records
BTO	Tube, Tracheostomy (W/Wo Connector)	2
FIH	Pump, Infusion Or Syringe, Extra-Luminal	1
FOZ	Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days	1
FSM	Tray, Surgical, Instrument	1
KYZ	Syringe, Irrigating (Non Dental)	1

Latest 510(k) clearances

Decided	510(k)	Device and applicant	Code
May 18, 1990	K901079	SINGLE-USE, STERILE 4OZ BOTTLE CONTAIN STER. WATER L H M Ent., Inc.	BTO
May 18, 1990	K901078	SINGLE-USE, STERILE 4OZ BOTTLE CONTAIN 0.9% SALINE L H M Ent., Inc.	BTO
Mar 15, 1990	K894610	CUSTOM TRAYS, KITS L H M Ent., Inc.	FSM
Feb 15, 1990	K900439	SINGLE-USE, STERILE, PREFILLED SYRINGE, 60CC L H M Ent., Inc.	FIH
Dec 15, 1989	K894611	CATHETER CARE KITS L H M Ent., Inc.	FOZ
Dec 13, 1988	K883506	IRRIGATION KIT L H M Ent., Inc.	KYZ

Latest recalls

Date	Firm and product	Code	Linked 510(k)
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