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

PANDA(R) NEEDLE CATHETER JEJUNOSTOMY TUBE

K Number: K891109 · Decision May 8, 1989
Classifications
1
FEI Numbers
228
Registration Numbers
229
Same Product Code
648
Applicant Total
83
Review Days
67

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Basic Information

Device Name
PANDA(R) NEEDLE CATHETER JEJUNOSTOMY TUBE
K Number
K891109
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5980
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Concept, Inc.
Date Received
March 2, 1989
Decision Date
May 8, 1989
Product Code
KNT
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

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

Product Code Device Name
KNT Tubes, Gastrointestinal (And Accessories)

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Other Clearances by Concept, Inc.

K Number Device Name
K912640 CONCEPT ENDOSTEAL FIXATION DEVICE
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K894929 STAPLE FIXATION SYSTEM
K892376 INTRAVISION(TM) ARTHROSCOPE SYSTEM (ADD'L APPLI.)
K881954 CONCEPT POWER SYSTEM
K884255 CONCEPT CCT-5200, THERMAL THERAPY SYSTEM
K882121 C-FLO SUCTION TUBE
K880414 TENDON HARVESTER
K874676 INTERFERENCE SCREW
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