
Accra Laboratories, Inc.
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COPPER SULFATE SOLUTION SP. GR.1.053 is an FDA 510(k)-cleared medical device (K803094) manufactured by Accra Laboratories, Inc.. This device is classified under the Clinical Toxicology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 5, 1981. Regulation: 8.