510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K924690Unknown

Various Non-Sterile Custom Trays/kits

Surgipro Central, Inc., Tarpon Springs FL / Traditional, Unknown
FDA source (opens on fda.gov)

K924690 is the FDA 510(k) clearance record for VARIOUS NON-STERILE CUSTOM TRAYS/KITS, a class II device, cleared for Surgipro Central, Inc. on under FDA product code MCY (Wound Dressing Kit). FDA's definition for product code MCY reads: "This product code has been established in accordance with the may 20, 1997, guidance entitled, convenience kits interim regulatory guidance, found at www.Fda.Gov/cdrh/ode/convkit.Html. This type of convenience kit, as listed in the...". FDA records list one 510(k) clearance for Surgipro Central, Inc. As of , FDA records show no recalls naming K924690.

Clearance record

Decision date
Received
(302 days to decision)
Product code
MCY Wound Dressing Kit
Regulation
21 CFR 880.5075
Device class
Class II
Review panel
General Hospital
Applicant
Surgipro Central, Inc. C/O Pat Lamb & Associates, Tarpon Springs FL
510(k) summary
Statement
Third party review
No

Clearances, product code MCY

Trailing 12 months

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

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