FDA 510(k) FDA class 2 Substantially Equivalent 🇳🇱 Netherlands

TrapIt

K Number: K191229 · Decision Jan 21, 2020
Classifications
1
FEI Numbers
276
Registration Numbers
277
Same Product Code
889
Applicant Total
8
Review Days
258

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Basic Information

Device Name
TrapIt
K Number
K191229
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1250
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Imds Operations B.V.
Date Received
May 8, 2019
Decision Date
January 21, 2020
Product Code
DQY
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
DQY Catheter, Percutaneous

Similar 510(k) Clearances

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

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Other Clearances by Imds Operations B.V.

K Number Device Name
K242337 FlowGuide (FG60F); GuidionShort (GS60F)
K241611 ShapeIT (SI014135)
K223728 Micro Rx
K210431 ReCross
K210110 Guidion
K200324 NHancer Rx
K121077 NHANCER