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FDA 510(k), K801758, MMI/GAELTEC CATHETER INTRAUTERINE
FDA 510(k), K801758, MMI/GAELTEC CATHETER INTRAUTERINE
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510(K) Number: K801758
Device Name: MMI/GAELTEC CATHETER INTRAUTERINE
Manufacturer: MEDICAL MEASUREMENTS, INC.
Device Classification Name: monitor, pressure, intrauterine
Regulation Number: 884.2700
Classification Product Code: KXO
Date Received: 07/28/1980
Decision Date: 08/14/1980
Regulation Medical Specialty: Obstetrics/Gynecology
Device Name: MMI/GAELTEC CATHETER INTRAUTERINE
Manufacturer: MEDICAL MEASUREMENTS, INC.
Device Classification Name: monitor, pressure, intrauterine
Regulation Number: 884.2700
Classification Product Code: KXO
Date Received: 07/28/1980
Decision Date: 08/14/1980
Regulation Medical Specialty: Obstetrics/Gynecology
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- 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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