510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K121929Substantially Equivalent

Zephyr 'X-Series Patient Transfer Sled

Diacor, Inc., West Valley City UT / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K121929 is the FDA 510(k) clearance record for ZEPHYR 'X-SERIES PATIENT TRANSFER SLED, a class II device, cleared for Diacor, Inc. on under FDA product code FRZ (Device, Patient Transfer, Powered). FDA records list 10 510(k) clearances for Diacor, Inc., from to . As of , FDA records show no recalls naming K121929.

Clearance record

Decision date
Received
(199 days to decision)
Product code
FRZ Device, Patient Transfer, Powered
Regulation
21 CFR 880.6775
Device class
Class II
Review panel
General Hospital
Applicant
Diacor, Inc. 2550 Decker Lake Blvd., West Valley City UT
510(k) summary
Summary PDF
Third party review
No

Clearances, product code FRZ

Trailing 12 months

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

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