FDA 510(k) FDA class 2 Substantially Equivalent 🇸🇪 Sweden

PRESSUREWIRE: AERIS AGILE TIP, AERIS AGILE TIP 300, CERTUS AGILE TIP, CERTUS AGILE TIP 300

K Number: K140466 · Decision Nov 13, 2014
Classifications
1
FEI Numbers
64
Registration Numbers
64
Same Product Code
63
Applicant Total
5
Review Days
262

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Basic Information

Device Name
PRESSUREWIRE: AERIS AGILE TIP, AERIS AGILE TIP 300, CERTUS AGILE TIP, CERTUS AGILE TIP 300
K Number
K140466
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2870
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
St. Jude Medical Systems AB
Date Received
February 24, 2014
Decision Date
November 13, 2014
Product Code
DXO
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

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

Product Code Device Name
DXO Transducer, Pressure, Catheter Tip

Similar 510(k) Clearances

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

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Other Clearances by St. Jude Medical Systems AB

K Number Device Name
K133587 PRESSUREWIRE AERIS AGILE TIP; PRESSUREWIRE AERIS AGILE TIP 300
K131452 PRESSUREWIRE; CERTUS, CERTUS 300, AERIS, AERIS 300
K111854 AO USB RECEIVER, WI-BOX, WI-BOX PSU KIT, WI-BOX XPRESS CABLE, PW USB RECEIVER
K110193 FEMOSTOP PLYS, FEMOSTOP HD, FEMOSTOP COMPRESSION ARCH; FEMOSTOP II PLUS SET; FEMOSTOP II PLUS ARCH, BILATERAL ADAPTER; F