ULTIMAT-SENSOR FOR BED OCCUPANCY MONITOR— 510(k) K942770

Name: FDA 510(k) clearance K942770
Creator: U.S. Food and Drug Administration
Published: 1994-12-23

Substantially Equivalent

Ultimate Development Corp.

FDA 510(k) clearance K942770 for ULTIMAT-SENSOR FOR BED OCCUPANCY MONITOR, Substantially Equivalent on 1994-12-23. Applicant: Ultimate Development Corp.. Device class: 1.

Clearance details

Applicant: Ultimate Development Corp.
Product code: Code KMI
Device class: Class 1
Regulation: 21 CFR 880.2400
Advisory panel: General Hospital
Date received: 1994-06-13
Decision date: 1994-12-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Tulsa, OK, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KMI

view all

K141877 — LEAF PATIENT MONITORING SYSTEM2014-11-10
K131585 — INTEL-GE CARE INNOVATIONS QUIETCARE2013-10-08
K130752 — DYNASENSE SYSTEM2013-08-15
K101109 — VIVATRAK2010-07-15
K090138 — MOBILECARE MONITOR, MODEL 21002009-04-24

Data sourced from openFDA. This site is unofficial and independent of the FDA.