510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K883390Substantially Equivalent

Pmd System-20

Datatek, Inc., Shreveport LA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K883390 is the FDA 510(k) clearance record for PMD SYSTEM-20, a class I device, cleared for Datatek, Inc. on under FDA product code KMI (Monitor, Bed Patient). FDA records list one 510(k) clearance for Datatek, Inc. As of , FDA records show no recalls naming K883390.

Clearance record

Decision date
Received
(77 days to decision)
Product code
KMI Monitor, Bed Patient
Regulation
21 CFR 880.2400
Device class
Class I
Review panel
General Hospital
Applicant
Datatek, Inc. 333 Southfield Rd., Shreveport LA
Third party review
No

Clearances, product code KMI

Trailing 12 months

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

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