FDA 510(k) Application Details - K051691

Device Classification Name Compressor, Air, Portable

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510(K) Number K051691
Device Name Compressor, Air, Portable
Applicant PRECISION MEDICAL, INC.
300 HELD DR.
NORTHAMPTON, PA 18067 US
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Contact JAMES PARKER
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Regulation Number 868.6250

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Classification Product Code BTI
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Date Received 06/23/2005
Decision Date 12/09/2005
Decision SESE - SUBST EQUIV
Classification Advisory Committee AN - Anesthesiology
Review Advisory Committee AN - Anesthesiology
Statement / Summary / Purged Status Summary
Type Traditional
Reviewed By Third Party N
Expedited Review



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