510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K830515Substantially Equivalent

Scotts Tap Water Substitute Concentrate

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

K830515 is the FDA 510(k) clearance record for SCOTTS TAP WATER SUBSTITUTE CONCENTRATE, a class I device, cleared for Surgipath Medical Industries, Inc. on under FDA product code KEQ (Media, Mounting, Water Soluble). FDA records list 30 510(k) clearances for Surgipath Medical Industries, Inc., from to . As of , FDA records show no recalls naming K830515.

Clearance record

Decision date
Received
(42 days to decision)
Product code
KEQ Media, Mounting, Water Soluble
Regulation
21 CFR 864.4010
Device class
Class I
Review panel
Pathology
Applicant
Surgipath Medical Industries, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code KEQ

Trailing 12 months

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

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