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

Zimmerman (Spectrophotometric), 17-Ketosteroids

21 CFR 862.1430 / Clinical Chemistry
FDA source (opens on fda.gov)

CCY is the FDA product code for Zimmerman (Spectrophotometric), 17-Ketosteroids, a class I device type, regulated under 21 CFR 862.1430. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
CCY
Device name
Zimmerman (Spectrophotometric), 17-Ketosteroids
Regulation
21 CFR 862.1430
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
1
Ingested recalls
0

Clearances, product code CCY

By decision year
1 clearance under product code CCY with a decision year between 1979 and 1979, 1979 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code CCY by decision year
YearClearances
19791

Applicants with the most clearances

Product code CCY
Applicants holding the most 510(k) clearances under product code CCY
ApplicantClearances
Hycel, 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 CCY.