The Tulip Mfg. Co. - FDA 510(k) Cleared Devices
Recent clearances: THE TULIP LAPAROSCOPE SHEATH 6MM SINGLE STOPCOCK, THE TULIP LAPAROSCOPE SHEATH 6MM DUAL STOPCOCK, THE TULIP MONO POLAR ROTATABLE ALLIGATOR FORCEP
24
Total
24
Cleared
0
Denied
FDA 510(k) Regulatory Record - The Tulip Mfg. Co. General & Plastic Surgery ✕
22 devices
Cleared
Jan 22, 1996
THE TULIP LAPAROSCOPE SHEATH 6MM SINGLE STOPCOCK
General & Plastic Surgery
213d
Cleared
Jan 22, 1996
THE TULIP LAPAROSCOPE SHEATH 6MM DUAL STOPCOCK
General & Plastic Surgery
210d
Cleared
Jan 17, 1996
THE TULIP MONO POLAR ROTATABLE ALLIGATOR FORCEP
General & Plastic Surgery
47d
Cleared
Jan 17, 1996
THE TULIP MONO POLAR ROTATABLE METZ SCISSORS
General & Plastic Surgery
47d
Cleared
Nov 14, 1995
THE TULIP COMPANY BRANSON #1 & #2 ELEVATOR
General & Plastic Surgery
144d
Cleared
Nov 14, 1995
THE TULIP COMPANY BRANSON POSTERIOR DISSECTOR
General & Plastic Surgery
144d
Cleared
Nov 14, 1995
THE TULIP COMPANY BRANSON #1 ELEVATOR
General & Plastic Surgery
141d
Cleared
Nov 14, 1995
THE TULIP COMPANY BRASON NERVE HOOK & DISSECTOR
General & Plastic Surgery
141d
Cleared
Nov 14, 1995
THE TULIP CXOMPANY BRANSON #2 ELEVATOR
General & Plastic Surgery
141d
Cleared
Nov 14, 1995
THE TULIP COMPANY BRANSON OVERSHEATH
General & Plastic Surgery
141d
Cleared
Oct 30, 1995
THE TULIP INSULATED SCISSORS
General & Plastic Surgery
129d
Cleared
Oct 30, 1995
THE TULIP COMPANY BRANSON SOFT TISSUE RETRACTOR
General & Plastic Surgery
129d