
Syntron Bioresearch, Inc.
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MIDSTREAM ONESTEP PREGNANCY HOME TEST is an FDA 510(k)-cleared medical device (K963341) manufactured by Syntron Bioresearch, Inc.. This device is classified under the Clinical Chemistry specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 1, 1996. Regulation: 8.