FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

THE TULIP COMPANY BRANSON #1 ELEVATOR

K Number: K952932 · Decision Nov 14, 1995
Classifications
1
FEI Numbers
573
Registration Numbers
573
Same Product Code
1391
Applicant Total
24
Review Days
141

Basic Information

Device Name
THE TULIP COMPANY BRANSON #1 ELEVATOR
K Number
K952932
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
THE TULIP MFG. CO.
Date Received
June 26, 1995
Decision Date
November 14, 1995
Product Code
GCJ
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
GCJ Laparoscope, General & Plastic Surgery

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Other Clearances by THE TULIP MFG. CO.

K Number Device Name
K952959 THE TULIP LAPAROSCOPE SHEATH 6MM DUAL STOPCOCK
K952906 THE TULIP LAPAROSCOPE SHEATH 6MM SINGLE STOPCOCK
K955502 THE TULIP MONO POLAR ROTATABLE METZ SCISSORS
K955501 THE TULIP MONO POLAR ROTATABLE ALLIGATOR FORCEP
K954734 THE TULIP LCI-200 ILLUMINATION & IMAGING SYSTEM (MODIFICATION)
K952958 THE TULIP COMPANY BRANSON OVERSHEATH
K952953 THE TULIP CXOMPANY BRANSON #2 ELEVATOR
K952902 THE TULIP COMPANY BRANSON POSTERIOR DISSECTOR
K952951 THE TULIP COMPANY BRASON NERVE HOOK & DISSECTOR
K952901 THE TULIP COMPANY BRANSON #1 & #2 ELEVATOR
Search all 24 clearances from THE TULIP MFG. CO. →