510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
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K924433Substantially Equivalent

Senior Tech Tabs 88 Trans Ra1/wra1/r1 Ann Type Cr1

Senior Technologies, Inc., Lincoln NE / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K924433 is the FDA 510(k) clearance record for SENIOR TECH TABS 88 TRANS RA1/WRA1/R1 ANN TYPE CR1, a class I device, cleared for Senior Technologies, Inc. on under FDA product code KMI (Monitor, Bed Patient). FDA records list one 510(k) clearance for Senior Technologies, Inc. As of , FDA records show no recalls naming K924433.

Clearance record

Decision date
Received
(296 days to decision)
Product code
KMI Monitor, Bed Patient
Regulation
21 CFR 880.2400
Device class
Class I
Review panel
General Hospital
Applicant
Senior Technologies, Inc. P.O. Box 80238, Lincoln NE
510(k) summary
Statement
Third party review
No

Clearances, product code KMI

Trailing 12 months

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

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