510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K834224Substantially Equivalent

Vacuum Regulator 0-2000 Mmhg Vr-1000

Trimeter Instrument Corp., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K834224 is the FDA 510(k) clearance record for VACUUM REGULATOR 0-2000 MMHG VR-1000, a class II device, cleared for Trimeter Instrument Corp. on under FDA product code KDP (Regulator, Vacuum). FDA records list one 510(k) clearance for Trimeter Instrument Corp. As of , FDA records show no recalls naming K834224.

Clearance record

Decision date
Received
(83 days to decision)
Product code
KDP Regulator, Vacuum
Regulation
21 CFR 880.6740
Device class
Class II
Review panel
General Hospital
Applicant
Trimeter Instrument Corp. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code KDP

Trailing 12 months

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

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