510(K) CLEARANCES 51 ▲2RECALLS POSTED 25 ▲2CLASS I 1PMA DECISIONS 50 ▲13WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K905788Substantially Equivalent

Model M1251a Mon. Full Disclosure Review System

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

K905788 is the FDA 510(k) clearance record for MODEL M1251A MON. FULL DISCLOSURE REVIEW SYSTEM, a class II device, cleared for Hewlett-Packard Co. on under FDA product code DXJ (Display, Cathode-Ray Tube, Medical). FDA records list 246 510(k) clearances for Hewlett-Packard Co., from to . As of , FDA records show no recalls naming K905788.

Clearance record

Decision date
Received
(161 days to decision)
Product code
DXJ Display, Cathode-Ray Tube, Medical
Regulation
21 CFR 870.2450
Device class
Class II
Review panel
Cardiovascular
Applicant
Hewlett-Packard Co. 175 Waltham St., Waltham MA
Third party review
No

Clearances, product code DXJ

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