510(k) K821321

SNYDER DEBRIBEMENT SYSTEM LDP-1 by Snyder Laboratories, Inc. — Product Code BTA

K821321 is an FDA 510(k) premarket notification submitted by Snyder Laboratories, Inc. for the device "SNYDER DEBRIBEMENT SYSTEM LDP-1". The FDA issued a decision of Substantially Equivalent on August 6, 1982. The device falls under product code BTA (Pump, Portable, Aspiration (Manual Or Powered)), a Class II device regulated under 21 CFR 878.4780. Snyder Laboratories, Inc. has at least 10 other 510(k) clearances on record.