FDA 510(k) FDA class 2 Substantially Equivalent 🇩🇰 Denmark

ULTRASOUND SCANNER, TYPE 1101

K Number: K002085 · Decision Aug 1, 2000
Classifications
1
FEI Numbers
348
Registration Numbers
349
Same Product Code
892
Applicant Total
4
Review Days
22

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Basic Information

Device Name
ULTRASOUND SCANNER, TYPE 1101
K Number
K002085
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
892.1560
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
B & K Medical A/S
Date Received
July 10, 2000
Decision Date
August 1, 2000
Product Code
IYO
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
IYO System, Imaging, Pulsed Echo, Ultrasonic

Similar 510(k) Clearances

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

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Other Clearances by B & K Medical A/S

K Number Device Name
K000567 ULTRASOUND SCANNER TYPE 2102
K991937 ULTRASOUND SCANNER, MODEL TYPE 2101
K936024 ULTRASOUND SCANNER 2001