510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K893406Substantially Equivalent

Deseret Prn Adapter

Deseret Medical, Inc., Sandy UT / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K893406 is the FDA 510(k) clearance record for DESERET PRN ADAPTER, a class I device, cleared for Deseret Medical, Inc. on under FDA product code KGZ (Accessories, Catheter). FDA records list 20 510(k) clearances for Deseret Medical, Inc., from to . As of , FDA records show no recalls naming K893406.

Clearance record

Decision date
Received
(51 days to decision)
Product code
KGZ Accessories, Catheter
Regulation
21 CFR 878.4200
Device class
Class I
Review panel
General, Plastic Surgery
Applicant
Deseret Medical, Inc. 9450 S. State St., Sandy UT
Third party review
No

Clearances, product code KGZ

Trailing 12 months

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

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