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

SUCCESS CECAL INTUBATION ASSIST, MODEL: 4100

K Number: K080764 · Decision May 6, 2008
Classifications
1
FEI Numbers
80
Registration Numbers
80
Same Product Code
71
Applicant Total
2
Review Days
49

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Basic Information

Device Name
SUCCESS CECAL INTUBATION ASSIST, MODEL: 4100
K Number
K080764
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Max Endoscopy, Inc.
Date Received
March 18, 2008
Decision Date
May 6, 2008
Product Code
ODC
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
ODC Endoscope Channel Accessory

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (ODC), ordered by most recent decision date.

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Other Clearances by Max Endoscopy, Inc.

K Number Device Name
K083275 PRECISION ENDOSCOPIC INFRARED COAGULATOR; MODEL 5100 SINGLE- USE DISPOSABLE MAXI-GUIDE FLEXIBLE LIGHTGUIDE; MODEL 5100-2