510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
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K930884Substantially Equivalent

Medical Procedure Tray, Modification

Enpak Medical Corp., Salt Lake City UT / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K930884 is the FDA 510(k) clearance record for MEDICAL PROCEDURE TRAY, MODIFICATION, cleared for Enpak Medical Corp. on under FDA product code LDQ. FDA records list one 510(k) clearance for Enpak Medical Corp. As of , FDA records show no recalls naming K930884.

Clearance record

Decision date
Received
(762 days to decision)
Product code
LDQ
Review panel
General Hospital
Applicant
Enpak Medical Corp. 2440 S. Progress Dr., Salt Lake City UT
510(k) summary
Statement
Third party review
No

Clearances, product code LDQ

Trailing 12 months

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

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