510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K910262Substantially Equivalent

Keller Vital Signs Monitor - Kms-890

Keller Medical Specialties Products, Inc., Antioch IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K910262 is the FDA 510(k) clearance record for KELLER VITAL SIGNS MONITOR - KMS-890, a class II device, cleared for Keller Medical Specialties Products, Inc. on under FDA product code DSJ (Alarm, Blood-Pressure). FDA records list 6 510(k) clearances for Keller Medical Specialties Products, Inc., from to . As of , FDA records show no recalls naming K910262.

Clearance record

Decision date
Received
(69 days to decision)
Product code
DSJ Alarm, Blood-Pressure
Regulation
21 CFR 870.1100
Device class
Class II
Review panel
Cardiovascular
Applicant
Keller Medical Specialties Products, Inc. 42609 Crawford Rd., Antioch IL
Third party review
No

Clearances, product code DSJ

Trailing 12 months

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

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