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

ENSTYLET MODELS EC0010, EC0020

K Number: K993376 · Decision Jan 5, 2000
Classifications
1
FEI Numbers
35
Registration Numbers
35
Same Product Code
27
Applicant Total
8
Review Days
90

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Basic Information

Device Name
ENSTYLET MODELS EC0010, EC0020
K Number
K993376
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1380
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Endocardial Solutions, Inc.
Date Received
October 7, 1999
Decision Date
January 5, 2000
Product Code
DRB
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
DRB Stylet, Catheter

Similar 510(k) Clearances

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

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Other Clearances by Endocardial Solutions, Inc.

K Number Device Name
K042493 ENSITE SYSTEM, MODEL EE3000
K033211 ENSITE SYSTEM
K030129 MODIFICATION TO ENSITE 3000 SYSTEM, MODEL EE3000
K012926 MODIFICATION TO ENSITE 3000 SYSTEM, MODEL EE3000
K001437 ENSITE 3000 SYSTEM, MODEL EE3000
K992479 ENSITE 3000 SYSTEM
K983456 ENSITE 3000 SYSTEM