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

CARDIOVASCULAR CUSTOM SURGICAL KIT

K Number: K844593 · Decision Jun 21, 1985
Classifications
1
FEI Numbers
273
Registration Numbers
273
Same Product Code
701
Applicant Total
9
Review Days
207

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Basic Information

Device Name
CARDIOVASCULAR CUSTOM SURGICAL KIT
K Number
K844593
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1340
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Xanmed Corp.
Date Received
November 26, 1984
Decision Date
June 21, 1985
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 Xanmed Corp.

K Number Device Name
K864623 OBSTETRICAL/GYNECOLOGICAL CUSTOM SURGICAL KIT
K844595 ORTHOPEDIC CUSTOM SURGICAL KIT
K844596 EMERGENCY ROOM & MINOR OFFICE PROCEDURE CUSTOM KIT
K844594 NEURO CUSTOM SURGICAL KIT
K851906 SURGICAL EYE PACK
K844597 MISCELLANEOUS GENERAL SURGICAL CUSTOM KIT
K843642 SUBCLAVIAN LEAD INTRODUCER SYS
K843641 CATHETER INTRODUCER SYSTEM