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

SONOCA 180/195 WOUND CARE SYSTEM

K Number: K072904 · Decision May 21, 2008
Classifications
1
FEI Numbers
115
Registration Numbers
116
Same Product Code
156
Applicant Total
1
Review Days
223

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
SONOCA 180/195 WOUND CARE SYSTEM
K Number
K072904
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Soering GmbH
Date Received
October 11, 2007
Decision Date
May 21, 2008
Product Code
LFL
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
LFL Instrument, Ultrasonic Surgical

Similar 510(k) Clearances

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

View all