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510(k) K873891

TISSUE CULTURE DISHES by Nunc, Inc. — Product Code KIZ

K873891 is an FDA 510(k) premarket notification submitted by Nunc, Inc. for the device "TISSUE CULTURE DISHES". The FDA issued a decision of Substantially Equivalent on November 25, 1987. The device falls under product code KIZ (Dish, Tissue Culture), a Class I device regulated under 21 CFR 864.2240. Nunc, Inc. has at least 4 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 25, 1987
Date Received
September 23, 1987
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Dish, Tissue Culture
Device Class
Class I
Regulation Number
864.2240
Review Panel
PA
Submission Type

Other clearances by Nunc, Inc.

  • K070047 — NUNC IVF DISHES AND NUNC IVF 4-WELL DISH (May 18, 2007)
  • K040717 — NUNC IVF MULTIDISH 4 WELLS NUNCLON (August 12, 2004)
  • K873889 — TISSUE CULTURE TUBES (November 25, 1987)
  • K873890 — TISSUE CULTURE FLASKS (November 25, 1987)

Other clearances for product code KIZ

  • K890542 — MULTIWELL CULTURE PLATE INSERTS (February 14, 1989)
  • K871483 — TISSUE CULTURE/BACTERIOLOGICAL PETRI DISHES (April 29, 1987)
  • K854724 — CEKK-ADHESIVE MATRIX-MULTIPLE WELL PLATE CAM-PLATE (December 13, 1985)
  • K853634 — CORNING CELL WELLS-MULTIPLE WELL PLATES (September 16, 1985)
  • K821687 — REMOVAWELL TISSUE CULTURE PLATE W/LID (June 24, 1982)
  • K790958 — 120 WELL HISTO-PLATE (June 28, 1979)
  • K781792 — PRESSURIZER, EXETER CEMENT (February 8, 1979)

FDA data resources