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FDA 510(k), K030379, APLAB, MODEL 801D0030
FDA 510(k), K030379, APLAB, MODEL 801D0030
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510(K) Number: K030379
Device Name: APLAB, MODEL 801D0030
Manufacturer: SECTOR MEDICAL CORP.
Device Classification Name: ventilatory effort recorder
Regulation Number: 868.2375
Classification Product Code: MNR
Date Received: 02/05/2003
Decision Date: 08/29/2003
Regulation Medical Specialty: Anesthesiology
Device Name: APLAB, MODEL 801D0030
Manufacturer: SECTOR MEDICAL CORP.
Device Classification Name: ventilatory effort recorder
Regulation Number: 868.2375
Classification Product Code: MNR
Date Received: 02/05/2003
Decision Date: 08/29/2003
Regulation Medical Specialty: Anesthesiology
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. IMPORTANT: The FDA FOIA office operations are currently suspended. We are happy to make the request but do not know when we will receive a response. Learn more about Fast-Track Requests here.
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