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FDA 510(k) Application Details - K021693
Device Classification Name
Chamber, Hyperbaric
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510(K) Number
K021693
Device Name
Chamber, Hyperbaric
Applicant
PAN-AMERICA HYPERBARICS, INC.
18111 COPPER RIDGE DR.
SAN ANTONIO, TX 78259-3612 US
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Contact
W.T. WORKMAN
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Regulation Number
868.5470
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Classification Product Code
CBF
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More FDA Info for this Product Code
Date Received
05/22/2002
Decision Date
10/24/2002
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
AN - Anesthesiology
Review Advisory Committee
AN - Anesthesiology
Statement / Summary / Purged Status
Summary
Type
Abbreviated
Reviewed By Third Party
N
Expedited Review
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