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

ENVINET(TM)

K Number: K874551 · Decision Jan 22, 1988
Classifications
1
FEI Numbers
59
Registration Numbers
59
Same Product Code
270
Applicant Total
38
Review Days
79

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Basic Information

Device Name
ENVINET(TM)
K Number
K874551
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent for Some Indications
Applicant
Marion Laboratories, Inc.
Date Received
November 4, 1987
Decision Date
January 22, 1988
Product Code
EFQ
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
EFQ Gauze/Sponge, Internal

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Other Clearances by Marion Laboratories, Inc.

K Number Device Name
K883391 POLYMER ADHESIVE BANDAGE
K875182 MODIFIED LABELING FOR TOXI-LAB THC SCREEN
K875181 MODIFIED LABELING FOR TOXI-LAB BROAD SPECTRUM
K874554 ENVICLUSIVE (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
K853073 CULTURETTE BRAND 10-MINUTE GROUP A STREP I.D.
Search all 38 clearances from Marion Laboratories, Inc. →