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

Nitroprusside Reaction (Qualitative, Urine), Cystine

21 CFR 862.1240 / Clinical Chemistry
FDA source (opens on fda.gov)

JLC is the FDA product code for Nitroprusside Reaction (Qualitative, Urine), Cystine, a class I device type, regulated under 21 CFR 862.1240. As of , FDA records hold 2 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
JLC
Device name
Nitroprusside Reaction (Qualitative, Urine), Cystine
Regulation
21 CFR 862.1240
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
2
Ingested recalls
0

Clearances, product code JLC

By decision year
2 clearances under product code JLC with a decision year between 1981 and 1985, 1981 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code JLC by decision year
YearClearances
19811
19851

Applicants with the most clearances

Product code JLC
Applicants holding the most 510(k) clearances under product code JLC
ApplicantClearances
Mission Pharmacal Company1
Sandare Chemical Co., 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 JLC.