The Tulip Mfg. Co. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
The Tulip Mfg. Co. - FDA 510(k) Cleared Devices
24
Total
24
Cleared
0
Denied
The Tulip Mfg. Co. has 24 FDA 510(k) cleared general & plastic surgery devices. Based in Mesa, US.
Historical record: 24 cleared submissions from 1995 to 1996.
Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - The Tulip Mfg. Co.
24 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
Nov 14, 1995
THE TULIP LCI-200 ILLUMINATION & IMAGING SYSTEM (MODIFICATION)
Gastroenterology & Urology
42d
Cleared
Oct 30, 1995
THE TULIP INSULATED SCISSORS
General & Plastic Surgery
129d