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510(k) K791334

MULTISCOPE by Amdia Medical Products — Product Code DQD

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 10, 1979
Date Received
July 20, 1979
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Stethoscope, Electronic
Device Class
Class II
Regulation Number
870.1875
Review Panel
CV
Submission Type

Other clearances by Amdia Medical Products

  • K791338 — DUAL HEAD STETHOSCOPE (August 10, 1979)
  • K791335 — NURSESCOPE (August 10, 1979)
  • K791333 — BOWLES STETHOSCOPE (August 10, 1979)
  • K791336 — BUCKS NEUROLOGICAL HAMMER (August 3, 1979)
  • K791337 — TAYLOR NEUROLOGICAL HAMMER (August 3, 1979)

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