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

N-Benzoyl-L-Tyrosine Ethyl Ester (U.V.), Chymotrypsin

21 CFR 862.1180 / Clinical Chemistry
FDA source (opens on fda.gov)

JKX is the FDA product code for N-Benzoyl-L-Tyrosine Ethyl Ester (U.V.), Chymotrypsin, a class I device type, regulated under 21 CFR 862.1180. As of , FDA records hold no 510(k) clearances under this code and no recalls.

Classification record

Product code
JKX
Device name
N-Benzoyl-L-Tyrosine Ethyl Ester (U.V.), Chymotrypsin
Regulation
21 CFR 862.1180
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
0
Ingested recalls
0

Companies listing this code with FDA

Companies whose registered establishments list this code