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

FLEXFINDER GUIDEWIRE

K Number: K942074 · Decision Jun 24, 1994
Classifications
1
FEI Numbers
38
Registration Numbers
38
Same Product Code
63
Applicant Total
20
Review Days
56

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Basic Information

Device Name
FLEXFINDER GUIDEWIRE
K Number
K942074
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5130
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Flexmedics
Date Received
April 29, 1994
Decision Date
June 24, 1994
Product Code
KNY
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
KNY Accessories, Catheter, G-U

Similar 510(k) Clearances

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

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Other Clearances by Flexmedics

K Number Device Name
K990765 FLEXFINDER GUIDE WIRE(REGULAR SHAFT/STIFF SHAFT) MARKED INK BANDS, FLEXFINDER GUIDE WIRE (REGULAR SHAFT/STIFF SHAFT) NO
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
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 →