Instrument, Coagulation
FDA product code KQG · 14 cleared devices
Class 2
Hematology
- Regulation
- 21 CFR 864.5400
- Review panel
- HE
- Implant
- No
- Life sustaining
- No
- Third party review
- Yes
- GMP exempt
- No
- Clearance span
- 1977-08-04 – 2005-08-16
KQG
2005-08-16
KQG
2002-10-25
FIBRON-1, FIBRON-4, QUIKCOAG, FIBRON
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KQG
1999-09-03
PACIFIC HEMOSTASIS THROMBOSCREEN 400C
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KQG
1999-06-21
PACIFIC HEMOSTASIS THROMBOSCREEN 200
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KQG
1999-05-03
HEMOCHRON RESPONSE
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KQG
1990-11-08
ELVI 828 DIGICLOT MULTISCAN
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KQG
1990-04-16
CLOT 2 SEMIAUTOMATIC COAGULATION ANALYZER
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KQG
1986-09-29
COAGULATOR (8 CHANNEL)
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KQG
1985-08-13
COAGULATOR
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KQG
1985-06-24
ELECTRA 800 AUTOMATIC COAGULATION TIMER
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KQG
1982-12-09
KOAGULAB 40-A AUTOMATED COAGULATION SYS
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KQG
1982-07-22
ELVI BICLOT 816
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KQG
1979-09-17
ELVI 810 CLOTSCANNER
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KQG
1977-08-04
INCUBATOR, PORTABLE, ACT-STAT
View details →No matching devices.
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