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FDA 510(k) Application Details - K983500
Device Classification Name
Analyzer, Gas, Oxygen, Gaseous-Phase
More FDA Info for this Device
510(K) Number
K983500
Device Name
Analyzer, Gas, Oxygen, Gaseous-Phase
Applicant
MEDICAL TECHNOLOGY SPECIALISTS, INC.
6290-D WARWICK RD.
RICHMOND, VA 23224 US
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Contact
DONALD W MORROW, III
Other 510(k) Applications for this Contact
Regulation Number
868.1720
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Classification Product Code
CCL
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More FDA Info for this Product Code
Date Received
10/06/1998
Decision Date
03/17/1999
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
AN - Anesthesiology
Review Advisory Committee
AN - Anesthesiology
Statement / Summary / Purged Status
Statement
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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