510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K060671Substantially Equivalent

Kvue Igrt Treatment Table Top, Rt-4551Kv, Kvue Inserts and Accessories, Various

Anholt Technologies Inc., Wyckoff NJ / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K060671 is the FDA 510(k) clearance record for KVUE IGRT TREATMENT TABLE TOP, RT-4551KV, KVUE INSERTS AND ACCESSORIES, VARIOUS, a class II device, cleared for Wfr/Aquaplast Corp. on under FDA product code JAI (Couch, Radiation Therapy, Powered). FDA records list 8 510(k) clearances for Anholt Technologies Inc., from to . As of , FDA records show no recalls naming K060671.

Clearance record

Decision date
Received
(51 days to decision)
Product code
JAI Couch, Radiation Therapy, Powered
Regulation
21 CFR 892.5770
Device class
Class II
Review panel
Radiology
Applicant
Wfr/Aquaplast Corp. 30 Lawlins Park, Wyckoff NJ
510(k) summary
Statement
Third party review
No

Clearances, product code JAI

Trailing 12 months

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

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