Tissuelink Medical, Inc.
Tissuelink Medical, Inc. holds FDA 510(k) medical device clearances, first cleared 2000, most recent 2008.
Top product codes for Tissuelink Medical, Inc.
Recent clearances by Tissuelink Medical, Inc.
- K073495 — TISSUELINK AQUAMANTYS MALLEABLE BIPOLAR SEALER WITH LIGHT
- K063639 — AQUAMANTYS SS4.0 BIPOLAR SEALER, MODEL 23-121-1
- K052859 — AQUAMANTYS PUMP GENERATOR SYSTEM
- K032132 — TISSUELINK FLOATING BALL MODEL 23-201-1
- K030380 — TISSUELINK SEALING FORCEPS, MODEL 1 21-202-1
- K022532 — TISSUELINK BIPOLAR FLOATING BALL DEVICE
- K020574 — TISSUELINK BIPOLAR FLOATING BALL DEVICE
- K014260 — TISSUELINK SOLID CYLINDER MONOPOLAR DEVICE
- K010661 — MODIFICATION TO TISSUELINK BIPOLAR FORCEPS
- K010662 — MODIFICATION TO TISSUELINK MONOPOLAR FLOATING BALL
- K003005 — TISSUELINK BIPOLAR FORCEPS
- K002680 — TISSUELINK MONOPOLAR FLOATING BALL'
Data sourced from openFDA. This site is unofficial and independent of the FDA.