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510(k) K932006

1500 SERIES REGULATOR by Precision Medical, Inc. — Product Code CAN

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 25, 1993
Date Received
April 21, 1993
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Regulator, Pressure, Gas Cylinder
Device Class
Class I
Regulation Number
868.2700
Review Panel
AN
Submission Type

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  • K921125 — AMBU OXYGEN REGULATOR (September 17, 1992)
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