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

Fluorometric Method, Triglycerides

21 CFR 862.1705 / Clinical Chemistry
FDA source (opens on fda.gov)

JGW is the FDA product code for Fluorometric Method, Triglycerides, a class I device type, regulated under 21 CFR 862.1705. As of , FDA records hold 3 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
JGW
Device name
Fluorometric Method, Triglycerides
Regulation
21 CFR 862.1705
Device class
Class I
Review panel
Clinical Chemistry
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
3
Ingested recalls
0

Clearances, product code JGW

By decision year
3 clearances under product code JGW with a decision year between 1978 and 1987, 1978 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code JGW by decision year
YearClearances
19781
19851
19871

Applicants with the most clearances

Product code JGW
Applicants holding the most 510(k) clearances under product code JGW
ApplicantClearances
Abbott Medical1
Boehringer Mannheim Corp.1
Sigma Chemical Co.1

Companies listing this code with FDA

Companies whose registered establishments list this code