Container, I.V.
FDA product code KPE · 117 cleared devices
Class 2
General Hospital
- Regulation
- 21 CFR 880.5025
- Review panel
- HO
- Implant
- No
- Life sustaining
- No
- Third party review
- Yes
- GMP exempt
- No
- Clearance span
- 1976-12-30 – 2026-04-02
KPE
1981-12-18
KPE
1981-11-02
SET FOR ASEPTIC DECANTING OF A FLEX I.V
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KPE
1981-09-16
IVA SEAL II
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KPE
1981-06-18
BOTTLE-TO-BOTTLE
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KPE
1981-06-18
I.V. BOTTLE (RIDGID)
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KPE
1981-06-17
I.V. PLASTIC BAG
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KPE
1981-06-16
GLASS VIALS
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KPE
1981-06-12
INSTAFIL
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KPE
1981-01-07
I.V. ADDITIVE CAP
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KPE
1980-08-27
TOTAL PARENTERAL NUTRITION SET BAG
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KPE
1979-10-26
LIFE CARE 1000ML.EMP. CONT. W/AT. Y-TRAN
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KPE
1979-10-01
ADDITIVE HINGE CAP
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KPE
1979-06-01
CAP, TAMPER PROOF PLASTIC
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KPE
1977-09-28
HICALIQ IVH BAG
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KPE
1977-08-03
EMPTY ADMIXTURE CONTAINERS
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KPE
1977-08-02
LIFECARE EMPTY CONTAINER
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KPE
1976-12-30
ADDITIVE CAP (2B8905)
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