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

CLEARVIEW BLOWER/MISTER

K Number: K973485 · Decision Dec 8, 1997
Classifications
1
FEI Numbers
146
Registration Numbers
146
Same Product Code
52
Applicant Total
56
Review Days
84

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Basic Information

Device Name
CLEARVIEW BLOWER/MISTER
K Number
K973485
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5475
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Dlp, Inc.
Date Received
September 15, 1997
Decision Date
December 8, 1997
Product Code
FQH
Advisory Committee
General Hospital
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
FQH Lavage, Jet

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