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FDA 510(k), K040723, MICROLIFE ELECTRONIC PEAK FLOW MONITOR, WITH PEF AND FEV1, MODELS PF-100 AND PF-100-1 (WITH SOFTWARE)
FDA 510(k), K040723, MICROLIFE ELECTRONIC PEAK FLOW MONITOR, WITH PEF AND FEV1, MODELS PF-100 AND PF-100-1 (WITH SOFTWARE)
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510(K) Number: K040723
Device Name: MICROLIFE ELECTRONIC PEAK FLOW MONITOR, WITH PEF AND FEV1, MODELS PF-100 AND PF-100-1 (WITH SOFTWARE)
Manufacturer: MICROLIFE INTELLECTUAL PROPERTY GMBH
Device Classification Name: meter, peak flow, spirometry
Regulation Number: 868.1860
Classification Product Code: BZH
Date Received: 03/22/2004
Decision Date: 06/10/2004
Regulation Medical Specialty: Anesthesiology
Device Name: MICROLIFE ELECTRONIC PEAK FLOW MONITOR, WITH PEF AND FEV1, MODELS PF-100 AND PF-100-1 (WITH SOFTWARE)
Manufacturer: MICROLIFE INTELLECTUAL PROPERTY GMBH
Device Classification Name: meter, peak flow, spirometry
Regulation Number: 868.1860
Classification Product Code: BZH
Date Received: 03/22/2004
Decision Date: 06/10/2004
Regulation Medical Specialty: Anesthesiology
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
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