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510(k) Data Aggregation
K Number
K011176Device Name
REUSABLE GLASS SYRINGES
Manufacturer
Date Cleared
2001-08-10
(115 days)
Product Code
Regulation Number
880.5860Why did this record match?
Applicant Name (Manufacturer) :
LOCKETT MEDICAL CORP.
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
Intended Use
Device Description
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K Number
K954887Device Name
STERILE WATER O.9% STERILE SALINE
Manufacturer
Date Cleared
1996-01-24
(100 days)
Product Code
Regulation Number
880.5200Why did this record match?
Applicant Name (Manufacturer) :
LOCKETT MEDICAL CORP.
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
Intended Use
Device Description
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