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510(k) K001412

PM 1800 CONSERVING DEVICE by Precision Medical, Inc. — Product Code NFB

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 20, 2001
Date Received
May 4, 2000
Clearance Type
Abbreviated
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Conserver, Oxygen
Device Class
Class II
Regulation Number
868.5905
Review Panel
AN
Submission Type

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  • K041122 — PRECISION LIQUID OXYGEN SYSTEM (October 4, 2004)

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