FDA 510(k) FDA unclassified Substantially Equivalent 🇺🇸 United States

I.V. START KIT

K Number: K780222 · Decision Mar 28, 1978
Classifications
1
FEI Numbers
402
Registration Numbers
403
Same Product Code
861
Applicant Total
38
Review Days
47

Basic Information

Device Name
I.V. START KIT
K Number
K780222
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Applicant
MARION LABORATORIES, INC.
Date Received
February 9, 1978
Decision Date
March 28, 1978
Product Code
FRO
Advisory Committee
Unknown
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
FRO Dressing, Wound, Drug

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K874554 ENVICLUSIVE (TM)
K874551 ENVINET(TM)
K874552 ENVISAN PAD
K874553 ENVISAN PASTE
K870864 CULTURETTE BRAND CDT CLOSTRIDIUM DIFFICILE TEST
K863485 MODIFICATION OF CDT(TM) CLOSTRIDIUM TEST
K862123 BIOSPHERE ANAEROBIC ENVIRONMENTAL DEVICE
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