510(k) K902917

PRECISION MEDICAL ELIMINATOR by Precision Medical, Inc. — Product Code BXY

K902917 is an FDA 510(k) premarket notification submitted by Precision Medical, Inc. for the device "PRECISION MEDICAL ELIMINATOR". The FDA issued a decision of Substantially Equivalent on July 23, 1990. The device falls under product code BXY (Flowmeter, Calibration, Gas), a Class I device regulated under 21 CFR 868.2350. Precision Medical, Inc. has at least 10 other 510(k) clearances on record.