510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K152585Substantially Equivalent

Resmon PRO FULL

Medical Graphics Corp., St. Paul MN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K152585 is the FDA 510(k) clearance record for Resmon PRO FULL, a class II device, cleared for Medical Graphics Corp. on under FDA product code PNV (Impedance Measuring Device Utilizing Oscillation Techniques). FDA's definition for product code PNV reads: "This device measures respiratory impedance". FDA records list 25 510(k) clearances for Medical Graphics Corp., from to . As of , FDA records show no recalls naming K152585.

Clearance record

Decision date
Received
(288 days to decision)
Product code
PNV Impedance Measuring Device Utilizing Oscillation Techniques
Regulation
21 CFR 868.1840
Device class
Class II
Review panel
Anesthesiology
Applicant
Medical Graphics Corp. 350 Oak Grove Pkwy., St. Paul MN
510(k) summary
Summary PDF
Third party review
No

Clearances, product code PNV

Trailing 12 months

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

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