FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

SYVEK PATCH

K Number: K972914 · Decision Dec 22, 1997
Classifications
1
FEI Numbers
972
Registration Numbers
972
Same Product Code
186
Applicant Total
8
Review Days
137

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Basic Information

Device Name
SYVEK PATCH
K Number
K972914
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.5240
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Marine Polymer Technologies, Inc.
Date Received
August 7, 1997
Decision Date
December 22, 1997
Product Code
KGX
Advisory Committee
General Hospital
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
KGX Tape And Bandage, Adhesive

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (KGX), ordered by most recent decision date.

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Other Clearances by Marine Polymer Technologies, Inc.

K Number Device Name
K160695 Talymed Suspension
K111524 MP 719
K082703 MRDH BANDAGE
K070557 MP 719
K053300 SYVEKEXCEL
K002550 RDH BANDAGE
K984177 MODIFICATION TO SKVEKPATCH