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

FLEXFINDER GUIDE WIRE(REGULAR SHAFT/STIFF SHAFT) MARKED INK BANDS, FLEXFINDER GUIDE WIRE (REGULAR SHAFT/STIFF SHAFT) NO

K Number: K990765 · Decision Mar 15, 1999
Classifications
1
FEI Numbers
91
Registration Numbers
91
Same Product Code
42
Applicant Total
20
Review Days
7

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Basic Information

Device Name
FLEXFINDER GUIDE WIRE(REGULAR SHAFT/STIFF SHAFT) MARKED INK BANDS, FLEXFINDER GUIDE WIRE (REGULAR SHAFT/STIFF SHAFT) NO
K Number
K990765
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Flexmedics
Date Received
March 8, 1999
Decision Date
March 15, 1999
Product Code
OCY
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
OCY Endoscopic Guidewire, Gastroenterology-Urology

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Other Clearances by Flexmedics

K Number Device Name
K964955 FLEXFINDER GUIDEWIRE (REGULAR SHAFT/STIFF SHAFT) MARKED INK BANDS ENCAP+/GUIDEWIRE(REGULAR SHAFT/STIFF SHAFT) NO MARKING
K952430 FINESSE GUIDEWIRE CORONARY
K943390 FLEXFINDER GUIDEWIRE
K942074 FLEXFINDER GUIDEWIRE
K934265 FLEXMEDICS SUPER-SEVEN STRANDED NICKEL-TITANIUM ARCHWIRE
K912843 FLEXMEDICS RETRACT ORTH PROBE, PETTINE BONE PROBE
K910674 FLEXMEDICS MALLEABLE CANNULA
K895899 FLEXMEDICS GUIDEWIRE .012 ONLY
K893626 FLEXMEDICS GUIDEWIRE
K885086 TIN COATED NITI ORTHODONTIC ARCH WIRES
Search all 20 clearances from Flexmedics →