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

LICHEN, BACTERIAL IN LINE BREATHING FILTER

K Number: K980662 · Decision Sep 14, 1998
Classifications
1
FEI Numbers
141
Registration Numbers
141
Same Product Code
201
Applicant Total
8
Review Days
206

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Basic Information

Device Name
LICHEN, BACTERIAL IN LINE BREATHING FILTER
K Number
K980662
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5260
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Dhd Healthcare Corp.
Date Received
February 20, 1998
Decision Date
September 14, 1998
Product Code
CAH
Advisory Committee
Anesthesiology
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
CAH Filter, Bacterial, Breathing-Circuit

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