Promedical , Ltd.

Promedical , Ltd. holds 5 FDA 510(k) medical device clearances, first cleared 1994, most recent 1995.

Top product codes for Promedical , Ltd.

FCG — Gastroenterology, Urology3 devices
GDF — General, Plastic Surgery1 device
LWE — Unknown1 device

Recent clearances by Promedical , Ltd.

K954596 — PRO-B CORE-RECT COAXIAL BIOPSY SYSTEMCode FCG·1995-10-07
K952350 — JAMSHIDI STYLE BIOPSY NEEDLE (ACRI) (BIOMID), ILLINOIS STYLE BIOPSY NEEDLE (ISAN)Code LWE·1995-07-17
K951598 — PRO-B BIOPSY NEEDLECode FCG·1995-04-21
K944944 — CHIBA, FRANSEEN, WESTCOTT, SPINAL STYLE ASPIRATION BIOPSY NEEDLECode FCG·1994-12-21
K944942 — BREAST LESION LOCALIZATION NEEDLECode GDF·1994-11-04

Data sourced from openFDA. This site is unofficial and independent of the FDA.