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510(k) K923771

PULSE RF TEST by Pulse Scientific, Inc. — Product Code DHR

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 5, 1992
Date Received
July 28, 1992
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
System, Test, Rheumatoid Factor
Device Class
Class II
Regulation Number
866.5775
Review Panel
IM
Submission Type

Other clearances by Pulse Scientific, Inc.

  • K923768 — PULSE CRP TEST (December 1, 1992)
  • K923767 — PULSE IM RED CELL TEST (October 16, 1992)

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