510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
JMDClass I

Radioimmunoassay, Total Estrogens, Nonpregnancy

21 CFR 862.1275 / Clinical Chemistry
FDA source (opens on fda.gov)

JMD is the FDA product code for Radioimmunoassay, Total Estrogens, Nonpregnancy, a class I device type, regulated under 21 CFR 862.1275. As of , FDA records hold 2 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
JMD
Device name
Radioimmunoassay, Total Estrogens, Nonpregnancy
Regulation
21 CFR 862.1275
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 JMD

By decision year
2 clearances under product code JMD with a decision year between 1978 and 1979, 1978 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code JMD by decision year
YearClearances
19781
19791

Applicants with the most clearances

Product code JMD
Applicants holding the most 510(k) clearances under product code JMD
ApplicantClearances
Environmental Sciences Assoc., Inc.1
Radioassay Systems Laboratories, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code