Medical Device Manufacturer · US , Palm Harbor , FL

L H M Ent., Inc. - FDA 510(k) Cleared Devices

6 submissions · 4 cleared · Since 1988

6

Total

4

Cleared

0

Denied

L H M Ent., Inc. has 4 FDA 510(k) cleared medical devices. Based in Palm Harbor, US.

Historical record: 4 cleared submissions from 1988 to 1990.

Browse the FDA 510(k) cleared devices submitted by L H M Ent., Inc. Filter by specialty or product code using the sidebar.

6 devices

1–6 of 6

SINGLE-USE, STERILE 4OZ BOTTLE CONTAIN 0.9% SALINE

K901078 · BTO Tube, Tracheostomy (w/wo Connector) · Anesthesiology

SINGLE-USE, STERILE 4OZ BOTTLE CONTAIN STER. WATER

K901079 · BTO Tube, Tracheostomy (w/wo Connector) · Anesthesiology

CUSTOM TRAYS, KITS

K894610 · FSM Tray, Surgical, Instrument · General & Plastic Surgery

SINGLE-USE, STERILE, PREFILLED SYRINGE, 60CC

K900439 · FIH Pump, Infusion Or Syringe, Extra-luminal · Gastroenterology & Urology

CATHETER CARE KITS

K894611 · FOZ Catheter, Intravascular, Therapeutic, Short-term Less Than 30 Days · General Hospital

K883506 · KYZ Syringe, Irrigating (non Dental) · General Hospital