Tillotson Healthcare Corp. is one of 16532 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Tillotson Healthcare Corp. - FDA 510(k) Cleared Devices
Recent clearances: ULTRA PRESERVE WITH ALOE VERA (GREEN) NATURAL RUBBER LATEX EXAMINATION GLOVE MADE FROM ALLOTEX AN ENZYME TREATED NATURAL, HPI SENSI GRIP STERILE POWDERED LATEX SURGICAL GLOVE,WITH LABELED PROTEIN CONTENT AND MADE FROM ALLOTEX AN ENZYME TREAT, TRUE ADVANTAGE NON-STERILE POWDER FREE PURPLE NITRILE EXAMINATION GLOVE
Tillotson Healthcare Corp. has 20 FDA 510(k) cleared general hospital devices. Based in Bedford, US.
Historical record: 20 cleared submissions from 1995 to 2002.
Browse the complete list of FDA 510(k) cleared general hospital devices from this manufacturer. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Tuv Product Service, Inc. as regulatory consultant.