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

ACUMEN SINGLE-LUMEN DELIVERY SHEATH

K Number: K053400 · Decision Jun 19, 2006
Classifications
1
FEI Numbers
273
Registration Numbers
273
Same Product Code
701
Applicant Total
12
Review Days
195

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Basic Information

Device Name
ACUMEN SINGLE-LUMEN DELIVERY SHEATH
K Number
K053400
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1340
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Acumen Medical, Inc.
Date Received
December 6, 2005
Decision Date
June 19, 2006
Product Code
DYB
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
DYB Introducer, Catheter

Similar 510(k) Clearances

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

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Other Clearances by Acumen Medical, Inc.

K Number Device Name
K083855 MODIFIED ACUMEN LEAD DELIVERY SHEATH WITH STYLET, MODEL: SPIRIT-10.5-59
K080500 MODIFICATION TO: ACUMEN SINGLE-LUMEN DELIVERY SHEATH, MODELS BLS-10, BLS-9, BLS-7
K070396 MODIFICATION TO: ACUMEN SINGLE-LUMEN DELIVERY SHEATH, MODELS BLS-8-45, BLS-7-45, BLS-6-45
K070051 ACUMEN INSIGHT ENDOCARDIAL VISUALIZATION SYSTEM
K070197 ACUMEN LEAD DELIVERY SHEATH WITH STYLET, MODELS LDS-10-64-STY AND LDS-10-57-STY
K062145 MODIFIED ACUMEN LEAD DELIVERY SHEATH, MODELS LDS-10-57, LDS-10-57-90, LDS-10-64 AND LDS-10-64-90
K062084 7F ACUMEN CORONARY SINUS VISUALIZATION SYSTEM, MODEL CSVS-7-67
K051515 MODIFIED ACUMEN SHEATH, MODEL TTW 10-65
K050015 MODIFIED ACUMEN SHEATH, MODEL TTWO767
K042381 CORONARY SINUS VISUALIZATION SYSTEM, MODEL CSVS5508
Search all 12 clearances from Acumen Medical, Inc. →