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

ERBELIFT HAND PUMP AND FLEXIBLE PROBE

K Number: K092090 · Decision Nov 30, 2009
Classifications
1
FEI Numbers
98
Registration Numbers
98
Same Product Code
88
Applicant Total
12
Review Days
139

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Basic Information

Device Name
ERBELIFT HAND PUMP AND FLEXIBLE PROBE
K Number
K092090
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Byrne Medical, Inc.
Date Received
July 14, 2009
Decision Date
November 30, 2009
Product Code
FBK
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
Y

Classifications

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

Product Code Device Name
FBK Endoscopic Injection Needle, Gastroenterology-Urology

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K102581 DEFENDO DISPOSABLE SUCTION VALVE MODEL 100305
K102409 DEFENDO DISPOSABLE AIR/WATER VALVE MODEL 100304
K093665 ENDO SMARTCAP
K092429 ENDOGATOR
K090851 DEFENDO (TM) BIOPSY VALVE FOR OLYMPUS(R) AND FUJINON(R) ENDOSCOPES, MODEL 100301, DEFENDO(TM) BIOPSY VALVE FOR PENTAX(R)
K060962 ENDOGATOR ENDOSCOPY IRRIGATION PUMP, MODEL EGP-100
K033695 IRRIGATION CHANNEL TUBING, MODEL 100135
Search all 12 clearances from Byrne Medical, Inc. →