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510(k) K873890

TISSUE CULTURE FLASKS by Nunc, Inc. — Product Code KJA

K873890 is an FDA 510(k) premarket notification submitted by Nunc, Inc. for the device "TISSUE CULTURE FLASKS". The FDA issued a decision of Substantially Equivalent on November 25, 1987. The device falls under product code KJA (Flask, 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
Flask, 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)
  • K873891 — TISSUE CULTURE DISHES (November 25, 1987)

Other clearances for product code KJA

  • K972404 — VACUTAINER BRAND SAFETY BLOOD COLLECTION ASSEMBLY(MULTIPLE) (July 22, 1997)
  • K933228 — KAPTON PEEL POUCH (March 30, 1994)
  • K885121 — CELL SCRAPER (December 28, 1988)
  • K873889 — TISSUE CULTURE TUBES (November 25, 1987)
  • K871324 — DU PONT STERICELL CELL CULTURE SYSTEM (April 14, 1987)
  • K870865 — TISSUE CULTURE BAG (March 30, 1987)
  • K864021 — TISSUE CULTURE FLASK (October 29, 1986)
  • K862152 — TISSUE CULTURE FLASK PL 732 PLASTIC ACCESSORY PROD (June 16, 1986)
  • K861253 — TISSUE CULTURE FLASK PL 732 PLASTIC (April 11, 1986)
  • K853441 — FETAL BOVINE SERUM IN TRANSFER CONTAINER (August 26, 1985)

FDA data resources