Atlas FDA

ENSTYLET MODELS EC0010, EC0020

FDA 510(k) clearance K993376 · decided 2000-01-05

Clearance details

K-number
K993376
Device name
ENSTYLET MODELS EC0010, EC0020
Applicant
Endocardial Solutions, Inc.
Decision
Substantially Equivalent
Date received
1999-10-07
Decision date
2000-01-05
Days to decision
90 days
Clearance type
Traditional
Product code
DRB
Device class
2
Regulation number
870.1380
Medical specialty
Cardiovascular
Advisory committee
Cardiovascular
Location
St. Paul, MN, US
Third-party review
No
Expedited review
No

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MOND RVOT STYLET MODELS 4140, 4141, 4150, 4151 (K080924)St. Jude Medical, Cardiac Rhythm Management Divisi2008-04-30
ST. JUDE MEDICAL, CPS DUO LEFT HEART LEAD DELIVERY SYSTEM (K072864)St. Jude Medical, Cardiac Rhythm Management Divisi2008-03-13
ACUITY STEERABLE STYLET ACCESSORY (K053019)Guidant Corporation2006-03-03
EASYTRAK 2 STYLET, MODELS 4826, 4829, 4832. (K052965)Guidant Corporation2006-02-13
SPECTRANETICS LLD CS, MODEL 518-039 (K043401)Spectranetics Corp.2005-03-16
STEERABLE STYLET (K040001)Synovis Surgical Innovations2004-03-09

Recalls involving this device

No recalls on record reference this clearance.