510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K832933Substantially Equivalent

Gold Film Mercury Analyzer #511

Jerome Instrument Corp., Walker MI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K832933 is the FDA 510(k) clearance record for GOLD FILM MERCURY ANALYZER #511, a class I device, cleared for Jerome Instrument Corp. on under FDA product code DPH (Mercury, Atomic Absorption). FDA records list one 510(k) clearance for Jerome Instrument Corp. As of , FDA records show no recalls naming K832933.

Clearance record

Decision date
Received
(87 days to decision)
Product code
DPH Mercury, Atomic Absorption
Regulation
21 CFR 862.3600
Device class
Class I
Review panel
Clinical Toxicology
Applicant
Jerome Instrument Corp. 4221 Richmond Rd., NW, Walker MI
Third party review
No

Clearances, product code DPH

Trailing 12 months

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

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