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510(k) K895484

STRATUS(R) GENTAMICIN FLUOROMETRIC ENZYME IMMUNO. by Baxter Healthcare Corp — Product Code LCD

K895484 is an FDA 510(k) premarket notification submitted by Baxter Healthcare Corp for the device "STRATUS(R) GENTAMICIN FLUOROMETRIC ENZYME IMMUNO.". The FDA issued a decision of Substantially Equivalent on October 4, 1989. The device falls under product code LCD (Enzyme Immunoassay, Gentamicin), a Class II device regulated under 21 CFR 862.3450. Baxter Healthcare Corp has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 4, 1989
Date Received
September 11, 1989
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Enzyme Immunoassay, Gentamicin
Device Class
Class II
Regulation Number
862.3450
Review Panel
TX
Submission Type

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Other clearances for product code LCD

  • K243500 — ARCHITECT iGentamicin (July 9, 2025)
  • K102699 — ARCHITECT IGENTAMICIN REAGENTS; ARCHITECT IGENTAMICIN CALIBRATORS (April 1, 2011)
  • K060709 — MULTIGENT GENTAMICIN (June 15, 2006)
  • K042479 — VITROS CHEMISTRY PRODUCTS GENT, TOBRA & VANC REAGENTS; VITROS CHEMISTYR PRODUCTS (January 6, 2005)
  • K020704 — ROCHE ONLINE GENTAMICIN (July 12, 2002)
  • K012978 — RANDOX GENTAMICIN (September 18, 2001)
  • K012311 — IMMULITE 2000 GENTAMICIN, MODELS L2KGE2 (200 TESTS), L2KGE6 (600 TESTS) (August 20, 2001)
  • K010984 — EMIT 2000 GENTAMICIN PLUS ASSAY (April 20, 2001)
  • K962819 — GENTAMICIN FLEX REAGENT CARTRIDGE (September 13, 1996)
  • K962519 — EMIT 2000 GENTAMICIN ASSAY AND CALIBRATORS (September 4, 1996)

FDA data resources