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510(k) K760486

HEMASTAIN WRIGHT STAIN by Geometric Data, Div. Smithkline Corp.

K760486 is an FDA 510(k) premarket notification submitted by Geometric Data, Div. Smithkline Corp. for the device "HEMASTAIN WRIGHT STAIN". The FDA issued a decision of Substantially Equivalent on August 30, 1976. Geometric Data, Div. Smithkline Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 30, 1976
Date Received
August 20, 1976
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Other clearances by Geometric Data, Div. Smithkline Corp.

  • K841852 — AUTOLYZER 800 (September 5, 1984)
  • K811534 — HEMASPINNER (August 18, 1981)
  • K791041 — HEMATRAK ABNORMAL RECOGNITION (September 4, 1979)
  • K791108 — CONTEXT FILTER (July 17, 1979)
  • K790816 — HEMATRAK MODEL 480 (July 17, 1979)
  • K790042 — STAIN, HEMASTAIN RETIC (February 15, 1979)
  • K780577 — PLATELETS/CU MM (May 19, 1978)
  • K772139 — RE-CELL SLIDE RECAP (January 5, 1978)
  • K761207 — HEMATRAK RBC MORPHOLOGY (October 18, 1977)
  • K770680 — HEMATRAK (July 1, 1977)

FDA data resources