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510(k) K810760

GILL'S HEMATOXYLIN #3 by Surgipath

K810760 is an FDA 510(k) premarket notification submitted by Surgipath for the device "GILL'S HEMATOXYLIN #3". The FDA issued a decision of Substantially Equivalent on April 14, 1981. Surgipath has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 14, 1981
Date Received
March 20, 1981
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Other clearances by Surgipath

  • K820027 — MODIFIED EA 50 (February 4, 1982)
  • K812940 — 10% NEUTRAL BUFFERED FORMALIN CONCENT (December 10, 1981)
  • K812087 — EA 50 (August 13, 1981)
  • K812086 — EA 65 (August 13, 1981)
  • K811825 — ORANGE G-6 (July 10, 1981)
  • K811826 — EOSIN Y (July 10, 1981)
  • K810836 — DECALCIFIER II (April 23, 1981)
  • K810758 — GILL'S HEMATOXYLIN #1 (April 14, 1981)
  • K810759 — GILL'S HEMATOXYLIN #2 (April 14, 1981)
  • K810733 — HARRIS HEMATOXYLIN (April 14, 1981)

FDA data resources