510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K163280Substantially Equivalent

RP Lite 760R

MEGO AFEK AC Ltd., Kibbutz Afek, IL / Special, Substantially Equivalent
FDA source (opens on fda.gov)

K163280 is the FDA 510(k) clearance record for RP Lite 760R, a class II device, cleared for Mego Afek AC , Ltd. on under FDA product code IRP (Massager, Powered Inflatable Tube). FDA records list 17 510(k) clearances for Mego Afek AC , Ltd., from to . As of , FDA records show no recalls naming K163280.

Clearance record

Decision date
Received
(67 days to decision)
Product code
IRP Massager, Powered Inflatable Tube
Regulation
21 CFR 890.5650
Device class
Class II
Review panel
Physical Medicine
Applicant
Mego Afek AC , Ltd. Kibbutz Afek, Kibbutz Afek, IL
510(k) summary
Statement
Third party review
No

Clearances, product code IRP

Trailing 12 months
11 clearances under product code IRP in the twelve months to October 2026, April 2026 the highest month at 3.
Show the numbers
Monthly 510(k) clearances under FDA product code IRP, trailing twelve months
MonthClearances
November 20251
December 20250
January 20261
February 20260
March 20260
April 20263
May 20262
June 20261
July 20262
August 20261
September 20260
October 20260