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

ACTISORB* PLUS ACTIVATED CHARCOAL DRESS W/SILVER

K Number: K892851 · Decision Sep 26, 1989
Classifications
1
FEI Numbers
384
Registration Numbers
385
Same Product Code
702
Applicant Total
4
Review Days
161

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Basic Information

Device Name
ACTISORB* PLUS ACTIVATED CHARCOAL DRESS W/SILVER
K Number
K892851
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent for Some Indications
Applicant
Johnson & Johnson Patient Care, Inc.
Date Received
April 18, 1989
Decision Date
September 26, 1989
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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Other Clearances by Johnson & Johnson Patient Care, Inc.

K Number Device Name
K895431 JOHNSON & JOHNSON TUBE SECUREMENT DEVICE
K890545 NU-DERM HYDROCOLLOID DRESSING
K884749 JOHNSON & JOHNSON STERILE SPRAY TIP SYRINGE