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

PERCUTANEOUS SHEATH INTRODUCER TRAY

K Number: K834074 · Decision Mar 19, 1984
Classifications
1
FEI Numbers
273
Registration Numbers
273
Same Product Code
701
Applicant Total
13
Review Days
115

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Basic Information

Device Name
PERCUTANEOUS SHEATH INTRODUCER TRAY
K Number
K834074
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1340
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Packaging Technologies, Inc.
Date Received
November 25, 1983
Decision Date
March 19, 1984
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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Other Clearances by Packaging Technologies, Inc.

K Number Device Name
K881756 STERILE SURGEONS GLOVES
K863326 BONE MARROW TRAY
K861041 ENHANCE
K850544 SHAVE PREP TRAY
K850438 RENAL BIOPSY TRAY
K844613 GENERAL PURPOSE INSTRUMENT TRAYS SUTURE REMOVAL TR
K844611 SINGLE BASIN SET
K844614 IV START KIT
K844612 ACUTE HEMODIALYSIS TRAYS
K834073 CENTRAL VEIN CATHERIZATION TRAY CC-20
Search all 13 clearances from Packaging Technologies, Inc. →