Radioimmunoassay, 17-Hydroxyprogesterone
FDA product code JLX · 19 cleared devices
Class 1
Clinical Chemistry
- Regulation
- 21 CFR 862.1395
- Review panel
- CH
- Implant
- No
- Life sustaining
- No
- Third party review
- No
- GMP exempt
- No
- Clearance span
- 1977-10-21 – 2010-07-23
JLX
2010-07-23
JLX
2009-04-16
AUTODELFIA NEONATAL 17A-OH-PROGESTERONE KIT
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JLX
2008-01-29
ENZYME IMMUNOASSAY FOR THE DETECTION OF SALIVARY 17-A-HYDROXYPROGESTERONE
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JLX
2007-03-13
ACCUWELL 17-ALPHA-HYDROXYPROESTERONE ENZYME IMMUNOASSAY WITH MODELS 6015XX-ECAH
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JLX
2005-07-11
MODIFICATION TO: AUTODELFIA NEONATAL 17A-OH-PROGESTERONE L KIT
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JLX
2004-09-30
AUTODELFIA NEONATAL 17A-OH-PROGESTERONE KIT
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JLX
2004-09-30
DELFIA NEONATAL 17A-OH-PROGESTERONE KIT
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JLX
1998-02-09
BIO-RAD MICROPLATE 17-HYDROXYPROGESTERONE TEST
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JLX
1995-03-30
ACCUSCREEN 17-HYDROXYPROGESTERONE
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JLX
1994-12-28
NEOSCREEN ELISA HYDROXYPROGESTERONE
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JLX
1994-11-10
DSL ACTIVE 17A-OH PROGESTERONE RIA (DSL 5000)
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JLX
1991-06-25
DELFIA(R) 17 -OH-PROGESTERON KIT
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JLX
1991-06-18
NEONATAL BLOOD SPOT TEST 17-HYDROXPROG RADIO KIT
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JLX
1989-09-07
DSL 17A-OH PROGERSTERONE (DSL #6800)
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JLX
1989-02-23
17-ALPHA-HYDROXYPROGESTERONE (17-OH-P) NEO. RIA
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JLX
1988-02-11
COAT-A-COUNT NEONATAL 17-ALPHA HYDROXPROG RIA KIT
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JLX
1986-04-24
COAT-A-COUNT 17-ALPHA-HYDROXYPROGESTERONE RIA KIT
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JLX
1984-02-04
PROGESTERONE TEST SET 125I 17-OH
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JLX
1977-10-21
17-HYDROXYPROGESTERONE TEST SET
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