510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K781516Substantially Equivalent

Test System Tissue Cell Culture Slide

Zeus Scientific LLC, Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K781516 is the FDA 510(k) clearance record for TEST SYSTEM TISSUE CELL CULTURE SLIDE, a class I device, cleared for Zeus Scientific, Inc. on under FDA product code KIY (Chamber, Slide Culture). FDA records list 141 510(k) clearances for Zeus Scientific, Inc., from to . As of , FDA records show no recalls naming K781516.

Clearance record

Decision date
Received
(27 days to decision)
Product code
KIY Chamber, Slide Culture
Regulation
21 CFR 864.2240
Device class
Class I
Review panel
Hematology
Applicant
Zeus Scientific, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code KIY

Trailing 12 months

FDA records hold no clearances under product code KIY in the trailing twelve months.

FDA records show no clearances under product code KIY in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code KIY, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260