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510(k) Data Aggregation
K Number
K000599Device Name
VITALOGRAPH BASE STATION
Manufacturer
Date Cleared
2000-09-08
(199 days)
Product Code
Regulation Number
868.1840Why did this record match?
Applicant Name (Manufacturer) :
VITALOGRAPH, INC.
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
Intended Use
Device Description
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K Number
K991412Device Name
VITALOGRAPH MICRO
Manufacturer
Date Cleared
2000-02-04
(287 days)
Product Code
Regulation Number
868.1860Why did this record match?
Applicant Name (Manufacturer) :
VITALOGRAPH, INC.
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
Intended Use
The Vitalograph Micro Spirometer is intended to measure, FVC, FEVI, PEF and FEV1% in patients with respiratory conditions such as Asthma, COPD, etc.
Device Description
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