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

EXACTA PERCUTANEOUS INTRODUCER SHEATH

K Number: K941428 · Decision Jul 6, 1994
Classifications
1
FEI Numbers
268
Registration Numbers
268
Same Product Code
682
Applicant Total
120
Review Days
104

Basic Information

Device Name
EXACTA PERCUTANEOUS INTRODUCER SHEATH
K Number
K941428
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1340
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
OHMEDA MEDICAL
Date Received
March 24, 1994
Decision Date
July 6, 1994
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

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