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

MP 719

K Number: K070557 · Decision May 23, 2007
Classifications
1
FEI Numbers
384
Registration Numbers
385
Same Product Code
702
Applicant Total
8
Review Days
85

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Basic Information

Device Name
MP 719
K Number
K070557
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Marine Polymer Technologies, Inc.
Date Received
February 27, 2007
Decision Date
May 23, 2007
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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K160695 Talymed Suspension
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K002550 RDH BANDAGE
K984177 MODIFICATION TO SKVEKPATCH
K972914 SYVEK PATCH