FDA 510(k) FDA class 2 Unknown 🇺🇸 United States

TRACHEOSTOMY CARE KIT

K Number: K924243 · Decision Jun 16, 1993
Classifications
1
FEI Numbers
75
Registration Numbers
75
Same Product Code
108
Applicant Total
21
Review Days
296

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Basic Information

Device Name
TRACHEOSTOMY CARE KIT
K Number
K924243
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5800
Medical Specialty
Anesthesiology
Decision
Unknown
Statement or Summary
Statement
Applicant
Transidyne General Corp.
Date Received
August 24, 1992
Decision Date
June 16, 1993
Product Code
JOH
Advisory Committee
Anesthesiology
Review Advisory Committee
AN
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
JOH Tube Tracheostomy And Tube Cuff

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Other Clearances by Transidyne General Corp.

K Number Device Name
K961217 BODILY FLUID DISPOSAL KIT
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K950773 PROPHYLAXIS PACK
K950743 ORAL PROCEDURE PACK
K950449 SURGICAL BUR
K950403 SURGICAL SAW BLADES
K924811 I.V. START KIT
K922339 SUTURE REMOVAL KIT
K922041 PRIMARY SURGICAL DRESSING TRAY
K897133 MODEL 1050 - UMBILICAL CORD BLOOD SAMPLING KIT
Search all 21 clearances from Transidyne General Corp. →