510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K780261Substantially Equivalent

Coverslipper

Shandon, Inc., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K780261 is the FDA 510(k) clearance record for COVERSLIPPER, a class I device, cleared for Shandon, Inc. on under FDA product code KIM (Device For Sealing Microsections). FDA records list 5 510(k) clearances for Shandon, Inc., from to . As of , FDA records show no recalls naming K780261.

Clearance record

Decision date
Received
(61 days to decision)
Product code
KIM Device For Sealing Microsections
Regulation
21 CFR 864.3400
Device class
Class I
Review panel
Pathology
Applicant
Shandon, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code KIM

Trailing 12 months

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

FDA records show no clearances under product code KIM in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code KIM, 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