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
K981376Substantially Equivalent

Hewlett-Packard M1205a Viridia 24 CT

Hewlett-Packard Co., Andover MA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K981376 is the FDA 510(k) clearance record for HEWLETT-PACKARD M1205A VIRIDIA 24 CT, a class II device, cleared for Hewlett-Packard Co. on under FDA product code DSI (Detector And Alarm, Arrhythmia). FDA records list 246 510(k) clearances for Hewlett-Packard Co., from to . As of , FDA records show no recalls naming K981376.

Clearance record

Decision date
Received
(263 days to decision)
Product code
DSI Detector And Alarm, Arrhythmia
Regulation
21 CFR 870.1025
Device class
Class II
Review panel
Cardiovascular
Applicant
Hewlett-Packard Co. 3000 Minuteman Rd., Andover MA
510(k) summary
Summary
Third party review
No

Clearances, product code DSI

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