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FDA 510(k), K760699, MULTI-TEST
FDA 510(k), K760699, MULTI-TEST
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510(K) Number: K760699
Device Name: MULTI-TEST
Manufacturer: LINCOLN LABORATORIES, INC.
Device Classification Name: system, delivery, allergen and vaccine
Regulation Number:
Classification Product Code: LDH
Date Received: 09/22/1976
Decision Date: 12/30/1976
Regulation Medical Specialty:
Device Name: MULTI-TEST
Manufacturer: LINCOLN LABORATORIES, INC.
Device Classification Name: system, delivery, allergen and vaccine
Regulation Number:
Classification Product Code: LDH
Date Received: 09/22/1976
Decision Date: 12/30/1976
Regulation Medical Specialty:
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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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