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

DEUTSCH ANTI-BLOCKAGE WOUND DRAIN

K Number: K052286 · Decision Oct 21, 2005
Classifications
1
FEI Numbers
243
Registration Numbers
243
Same Product Code
76
Applicant Total
1
Review Days
60

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Basic Information

Device Name
DEUTSCH ANTI-BLOCKAGE WOUND DRAIN
K Number
K052286
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4200
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
The Catheter Exchange, Inc.
Date Received
August 22, 2005
Decision Date
October 21, 2005
Product Code
GBX
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
GBX Catheter, Irrigation

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