FDA 510(k) FDA class 2 Unknown 🇺🇸 United States

SNAP WOUND CARE DEVICE

K Number: DEN080011 · Decision Aug 7, 2009
Classifications
1
FEI Numbers
11
Registration Numbers
11
Same Product Code
16
Applicant Total
9
Review Days
277

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Basic Information

Device Name
SNAP WOUND CARE DEVICE
K Number
DEN080011
Device Class
FDA class 2
Clearance Type
Post-NSE
Regulation Number
878.4683
Medical Specialty
General, Plastic Surgery
Decision
Unknown
Applicant
Spiracur, Inc.
Date Received
November 3, 2008
Decision Date
August 7, 2009
Product Code
OKO
Advisory Committee
General, Plastic Surgery
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
OKO Negative Pressure Wound Therapy Non-Powered Suction Apparatus

Similar 510(k) Clearances

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

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Other Clearances by Spiracur, Inc.

K Number Device Name
K151710 SNaP Wound Care System
K142272 SNaP Wound Care System
K132080 SNAP WOUND CARE SYSTEM
K133137 CISNAP CLOSED INCISION SYSTEM
K113032 SNAP WOUND CARE SYSTEM
K112341 SNAP WOUND CARE SYSTEM
K111393 SNAP (R) WOUND CARE SYSTEM
K111006 CI-SNAP WOUND CARE SYSTEM