FDA 510(k) FDA class 1 Unknown 🇺🇸 United States

TRACHEAL SUCTION CATHETER

K Number: K935600 · Decision May 10, 1994
Classifications
1
FEI Numbers
257
Registration Numbers
257
Same Product Code
115
Applicant Total
24
Review Days
172

Basic Information

Device Name
TRACHEAL SUCTION CATHETER
K Number
K935600
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
868.6810
Medical Specialty
Anesthesiology
Decision
Unknown
Statement or Summary
Statement
Applicant
PURITAS HEALTH CARE, INC.
Date Received
November 19, 1993
Decision Date
May 10, 1994
Product Code
BSY
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
BSY Catheters, Suction, Tracheobronchial

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K940055 MULTISET
K940054 MEASURED VOLUME SOLUTION ADMINISTRATION SET
K935583 SUCTION SET, TRACHAEL
K935532 TRANSFER SET
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K940070 STOPCOCK INTRAVENOUS THERAPY
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