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510(k) K790673

OMNIMEDICAL AUTOMATIC 1001 by Omnimedical — Product Code IZL

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 4, 1979
Date Received
April 9, 1979
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
System, X-Ray, Mobile
Device Class
Class II
Regulation Number
892.1720
Review Panel
RA
Submission Type

Other clearances by Omnimedical

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  • K812393 — 4001 CT SCANNER (October 13, 1981)
  • K812400 — OMNIMEDICAL QUAD I (October 2, 1981)
  • K802206 — OMNI SCANNER CT 6000 (October 23, 1980)

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