FDA 510(k), K022124, GALEMED PEAK FLOW METER, MODELS 3751/3752
FDA 510(k), K022124, GALEMED PEAK FLOW METER, MODELS 3751/3752
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510(K) Number: K022124
Device Name: GALEMED PEAK FLOW METER, MODELS 3751/3752
Manufacturer: GALEMED CORP.
Device Classification Name: meter, peak flow, spirometry
Regulation Number: 868.1860
Classification Product Code: BZH
Date Received: 07/01/2002
Decision Date: 04/03/2003
Regulation Medical Specialty: Anesthesiology
Device Name: GALEMED PEAK FLOW METER, MODELS 3751/3752
Manufacturer: GALEMED CORP.
Device Classification Name: meter, peak flow, spirometry
Regulation Number: 868.1860
Classification Product Code: BZH
Date Received: 07/01/2002
Decision Date: 04/03/2003
Regulation Medical Specialty: Anesthesiology
- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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