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

CENTRAL VEIN CATHERIZATION KIT W/WITHOUT MEDICA.

K Number: K870411 · Decision Jun 2, 1987
Classifications
1
FEI Numbers
276
Registration Numbers
277
Same Product Code
889
Applicant Total
3
Review Days
119

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Basic Information

Device Name
CENTRAL VEIN CATHERIZATION KIT W/WITHOUT MEDICA.
K Number
K870411
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1250
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Medical Surgical Concepts, Inc.
Date Received
February 3, 1987
Decision Date
June 2, 1987
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.

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Other Clearances by Medical Surgical Concepts, Inc.

K Number Device Name
K870413 PERCUTANEOUS SHEATH W/WO MEDI. (5,6,7,8,8.5FR)
K870412 TRIPLE LUMEN INFUSION CATHETERIZATION SET OR KIT