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

ASPIRATION PUMP, MODEL IMD-020

K Number: K041405 · Decision Sep 2, 2004
Classifications
1
FEI Numbers
98
Registration Numbers
98
Same Product Code
158
Applicant Total
3
Review Days
99

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Basic Information

Device Name
ASPIRATION PUMP, MODEL IMD-020
K Number
K041405
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4780
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Industrial & Medical Design, Inc.
Date Received
May 26, 2004
Decision Date
September 2, 2004
Product Code
BTA
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
BTA Pump, Portable, Aspiration (Manual Or Powered)

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K Number Device Name
K033072 LUCENTLITE, MODEL IMD 010
K992687 MILLENIUM MICROKERATOME, MODEL IMD-001