FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

ECOTRACT ADJUSTABLE WOUND PROTECTOR/RETRACTOR

K Number: K010711 · Decision May 22, 2001
Classifications
1
FEI Numbers
200
Registration Numbers
200
Same Product Code
449
Applicant Total
4
Review Days
74

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Basic Information

Device Name
ECOTRACT ADJUSTABLE WOUND PROTECTOR/RETRACTOR
K Number
K010711
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4370
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Advanced Surgical Concepts (Asc)
Date Received
March 9, 2001
Decision Date
May 22, 2001
Product Code
KKX
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
HO
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
KKX Drape, Surgical, Antimicrobial

Similar 510(k) Clearances

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

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Other Clearances by Advanced Surgical Concepts (Asc)

K Number Device Name
K011183 OMNIPORT HAND AND INSTRUMENT ACCESS DEVICE
K002013 OMNIPORT
K993544 SPACE-OR RETRACTOR