Atlas FDA

SLIM Microcatheter

FDA 510(k) clearance K260199 · decided 2026-07-13

Clearance details

K-number
K260199
Device name
SLIM Microcatheter
Applicant
Balt USA, LLC
Decision
Substantially Equivalent
Date received
2026-01-22
Decision date
2026-07-13
Days to decision
172 days
Clearance type
Traditional
Product code
QJP
Device class
2
Regulation number
870.1250
Medical specialty
Cardiovascular
Advisory committee
Cardiovascular
Location
Irvine, CA, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
Millipede88 Access Catheter (K253901)Perfuze, Ltd.2026-07-09
Trevo Trak 21 Microcatheter (K261889)Stryker Neurovascular2026-07-01
ISAAC Neurovascular Navigation Catheter (K261808)Microvention Inc. d/b/a Terumo Neuro2026-06-30
BOBBY Balloon Guide Catheter (K261549)MicroVention, Inc., d/b/a Terumo Neuro2026-06-09
Zenith Distal Access Long Sheath (K253359)Suzhou Zenith Vascular SciTech Limited2026-05-22
SAYA 86 Radial Access Guide Catheter (K254178)Asahi Intecc Co., Ltd.2026-05-11
BosCATH Support Catheter (K254046)Sonorous NV, Inc.2026-04-21
Next Generation 088 Catheter (K254223)Balt USA, LLC2026-04-16
PATH BGC (K260938)Crossroads Neurovascular, Inc.2026-04-15
Radical 6F Access Catheter (K253975)Maduro Medical, Inc.2026-04-09
AXS Lift Intracranial Base Catheter (K253032)Stryker Neurovascular2026-02-11
Toro 88 Superbore Catheter (K252297)Toro Neurovascular, Inc.2026-01-16

Recalls involving this device

No recalls on record reference this clearance.