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510(k) K131138

RESPIRE PINK SERIES - HERBST by Respire Medical — Product Code LRK

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 9, 2013
Date Received
April 23, 2013
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Device, Anti-Snoring
Device Class
Class II
Regulation Number
872.5570
Review Panel
DE
Submission Type

Other clearances by Respire Medical

  • K214096 — Respire Clear (May 31, 2022)
  • K111207 — RESPIRE BLUE SERIES (August 23, 2011)

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