510(K) CLEARANCES 51 ▲2RECALLS POSTED 25 ▲2CLASS I 1PMA DECISIONS 50 ▲13WEEK ENDING / FDA DATA AS OF
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K071564Substantially Equivalent

Motiva Monitor Device Connectivity, Model# 453564036921

Philips North America LLC, Andover MA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K071564 is the FDA 510(k) clearance record for MOTIVA MONITOR DEVICE CONNECTIVITY, MODEL# 453564036921, a class II device, cleared for Philips Medical Systems on under FDA product code DRG (Transmitters And Receivers, Physiological Signal, Radiofrequency). FDA records list 680 510(k) clearances for Philips North America LLC, from to . As of , FDA records show no recalls naming K071564.

Clearance record

Decision date
Received
(85 days to decision)
Product code
DRG Transmitters And Receivers, Physiological Signal, Radiofrequency
Regulation
21 CFR 870.2910
Device class
Class II
Review panel
Cardiovascular
Applicant
Philips Medical Systems 3000 Minuteman Rd., Andover MA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code DRG

Trailing 12 months
2 clearances under product code DRG in the twelve months to November 2026, January 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code DRG, trailing twelve months
MonthClearances
December 20250
January 20261
February 20260
March 20260
April 20260
May 20260
June 20260
July 20261
August 20260
September 20260
October 20260
November 20260