FDA 510(k) FDA unclassified Substantially Equivalent 🇺🇸 United States

LOCKETT MEDICAL CORP. GAUZE

K Number: K950404 · Decision Apr 17, 1995
Classifications
1
FEI Numbers
59
Registration Numbers
59
Same Product Code
270
Applicant Total
3
Review Days
76

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Basic Information

Device Name
LOCKETT MEDICAL CORP. GAUZE
K Number
K950404
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Lockett Medical Corp.
Date Received
January 31, 1995
Decision Date
April 17, 1995
Product Code
EFQ
Advisory Committee
Unknown
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
EFQ Gauze/Sponge, Internal

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