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

COUPLANT WARMING DEVICE

K Number: K893225 · Decision Oct 12, 1989
Classifications
1
FEI Numbers
348
Registration Numbers
349
Same Product Code
892
Applicant Total
6
Review Days
168

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Basic Information

Device Name
COUPLANT WARMING DEVICE
K Number
K893225
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1560
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
Echo Ultrasound
Date Received
April 27, 1989
Decision Date
October 12, 1989
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 Echo Ultrasound

K Number Device Name
K924054 PHONOCARDIOGRAPH
K903414 TRANSESOPHAGEAL PROBE HOLDER & DISINFECTING COLUMN
K872519 STERILIZED OMNI GEL
K844034 SONOCARE
K844120 ULTRASONIC SCANNER CALIBRATION & TEST OBJECTS