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

BLUE SKY BIO PLAN, VERSION .38

K Number: K090607 · Decision Apr 22, 2009
Classifications
1
FEI Numbers
609
Registration Numbers
609
Same Product Code
2221
Applicant Total
9
Review Days
47

Basic Information

Device Name
BLUE SKY BIO PLAN, VERSION .38
K Number
K090607
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.2050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
BLUE SKY BIO, LLC
Date Received
March 6, 2009
Decision Date
April 22, 2009
Product Code
LLZ
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

Classifications

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

Product Code Device Name
LLZ System, Image Processing, Radiological

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