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

Mercury, Atomic Absorption

21 CFR 862.3600 / Clinical Toxicology
FDA source (opens on fda.gov)

DPH is the FDA product code for Mercury, Atomic Absorption, a class I device type, regulated under 21 CFR 862.3600. As of , FDA records hold 2 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
DPH
Device name
Mercury, Atomic Absorption
Regulation
21 CFR 862.3600
Device class
Class I
Review panel
Clinical Toxicology
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
Yes
Ingested clearances
2
Ingested recalls
0

Clearances, product code DPH

By decision year
2 clearances under product code DPH with a decision year between 1978 and 1983, 1978 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code DPH by decision year
YearClearances
19781
19831

Applicants with the most clearances

Product code DPH
Applicants holding the most 510(k) clearances under product code DPH
ApplicantClearances
Jerome Instrument Corp.1
Revvity Health Sciences, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

No registered establishment in MDM’s records lists product code DPH.