FDA 510(k), K851082, V. MUELLER BLOM-SINGER ESOPHAGEAL INSUFFLATION TES
FDA 510(k), K851082, V. MUELLER BLOM-SINGER ESOPHAGEAL INSUFFLATION TES
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510(K) Number: K851082
Device Name: V. MUELLER BLOM-SINGER ESOPHAGEAL INSUFFLATION TES
Manufacturer: AMERICAN V. MUELLER
Device Classification Name: catheter, nasopharyngeal
Regulation Number: 874.4175
Classification Product Code: ENW
Date Received: 03/18/1985
Decision Date: 07/22/1985
Regulation Medical Specialty: Ear Nose & Throat
Device Name: V. MUELLER BLOM-SINGER ESOPHAGEAL INSUFFLATION TES
Manufacturer: AMERICAN V. MUELLER
Device Classification Name: catheter, nasopharyngeal
Regulation Number: 874.4175
Classification Product Code: ENW
Date Received: 03/18/1985
Decision Date: 07/22/1985
Regulation Medical Specialty: Ear Nose & Throat
- 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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