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

LABORIE INJETAK ADJUSTABLE TIP NEEDLE, FLEXIBLE TIP AND RIDGID TIP

K Number: K090830 · Decision Jul 21, 2009
Classifications
1
FEI Numbers
98
Registration Numbers
98
Same Product Code
88
Applicant Total
11
Review Days
117

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Basic Information

Device Name
LABORIE INJETAK ADJUSTABLE TIP NEEDLE, FLEXIBLE TIP AND RIDGID TIP
K Number
K090830
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Laborie Medical Technologies, Ltd.
Date Received
March 26, 2009
Decision Date
July 21, 2009
Product Code
FBK
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
FBK Endoscopic Injection Needle, Gastroenterology-Urology

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Other Clearances by Laborie Medical Technologies, Ltd.

K Number Device Name
K962009 UROSTYM
K955856 TEX-AID BLUE
K955810 U-TEX
K951805 PIPER, MODEL NUMBER UDS-PIPERB
K942563 ELITE BIOFEEDBACK
K942023 INFUSION PUMP, MODEL NO. UDP-5
K934369 DRI SLEEPER
K931574 ADVANCE MODEL UDS-ADV
K930005 DRITRAINER
K924086 NICKI, MODEL NUMBER USD-NK-UP1
Search all 11 clearances from Laborie Medical Technologies, Ltd. →