510(k) K951125

LIFEFORCE CLINICAL HYPERBARIC FACILITY by Reimers Systems, Inc. — Product Code CBF

K951125 is an FDA 510(k) premarket notification submitted by Reimers Systems, Inc. for the device "LIFEFORCE CLINICAL HYPERBARIC FACILITY". The FDA issued a decision of Substantially Equivalent on June 2, 1995. The device falls under product code CBF (Chamber, Hyperbaric), a Class II device regulated under 21 CFR 868.5470. Reimers Systems, Inc. has at least 4 other 510(k) clearances on record.