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

Acid, Phosphoric-Tungstic (Spectrophotometric), Chloride

21 CFR 862.1170 / Clinical Chemistry
FDA source (opens on fda.gov)

CHG is the FDA product code for Acid, Phosphoric-Tungstic (Spectrophotometric), Chloride, a class II device type, regulated under 21 CFR 862.1170. As of , FDA records hold 3 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
CHG
Device name
Acid, Phosphoric-Tungstic (Spectrophotometric), Chloride
Regulation
21 CFR 862.1170
Device class
Class II
Review panel
Clinical Chemistry
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
Yes
Ingested clearances
3
Ingested recalls
0

Clearances, product code CHG

By decision year
3 clearances under product code CHG with a decision year between 1990 and 1994, 1994 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code CHG by decision year
YearClearances
19901
19942

Applicants with the most clearances

Product code CHG
Applicants holding the most 510(k) clearances under product code CHG
ApplicantClearances
Sekisui Diagnostics P.E.I. Inc.1
Intersect Systems, Inc.1
Synermed, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code