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

Amplatzer Piccolo™ Delivery System (9-PDS-04F-045)

K Number: K252417 · Decision Dec 17, 2025
Classifications
1
FEI Numbers
276
Registration Numbers
277
Same Product Code
889
Applicant Total
57
Review Days
138

Basic Information

Device Name
Amplatzer Piccolo™ Delivery System (9-PDS-04F-045)
K Number
K252417
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1250
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
ABBOTT MEDICAL
Date Received
August 1, 2025
Decision Date
December 17, 2025
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.

View all

Other Clearances by ABBOTT MEDICAL

K Number Device Name
K253459 OPTIS Mobile Next Imaging System (1014932); OPTIS Integrated Next Imaging System (1014933); Ultreon 3.0 Software Upgrade Kit (ULTR300001)
K260212 EnSite™ X EP System
K253907 Disposable Radiofrequency Cannula
K260499 Amplatzer™ Trevisio™ Intravascular Delivery System; 9-ATV06F45/609-ATV07F45/609-ATV07F45/809-ATV08F45/609-ATV08F45/809-ATV09F45/809-ATV10F45/809-ATV12F45/80
K252512 Armada™ 14 NC PTA Catheter
K253516 Assert-IQ (DM5100)
K253232 Seguin Annuloplasty Ring
K250031 Amplatzer Guidewire
K252013 EnSite™ X EP System
K251463 EnSite™ X EP System, AutoMark Index Software License (ENSITE-AMI-01); EnSite™ X EP System, AutoMark Index Temporary Software License (ENSITE-D-AMI-01)
Search all 57 clearances from ABBOTT MEDICAL →