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510(k) K823350

ELASTIC COMPRESSION ANKLET by Podiatry Products Corp. — Product Code FQL

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 3, 1982
Date Received
November 9, 1982
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Stocking, Medical Support (For General Medical Purposes)
Device Class
Class I
Regulation Number
880.5780
Review Panel
HO
Submission Type

Other clearances for product code FQL

  • K944240 — SOFT SOCK (December 27, 1994)
  • K823789 — ELASTIC COMPRESSION ANKLET (January 7, 1983)
  • K821260 — VITOFIT (June 23, 1982)
  • K821259 — VITASAN (June 23, 1982)
  • K820484 — VENES CUSTON RX (March 18, 1982)