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FDA 510(k), K932122, BIOMIC VIDEO PLATE READER
FDA 510(k), K932122, BIOMIC VIDEO PLATE READER
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510(K) Number: K932122
Device Name: BIOMIC VIDEO PLATE READER
Manufacturer: GILES SCIENTIFIC, INC.
Device Classification Name: reader, zone, automated
Regulation Number: 866.2850
Classification Product Code: KZK
Date Received: 05/03/1993
Decision Date: 03/01/1994
Regulation Medical Specialty: Microbiology
Device Name: BIOMIC VIDEO PLATE READER
Manufacturer: GILES SCIENTIFIC, INC.
Device Classification Name: reader, zone, automated
Regulation Number: 866.2850
Classification Product Code: KZK
Date Received: 05/03/1993
Decision Date: 03/01/1994
Regulation Medical Specialty: Microbiology
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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. Learn more about Fast-Track Requests here.
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