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

CTS-3060 AUTOMATED SEMEN ANALYZER

K Number: K881765 · Decision Feb 15, 1989
Classifications
1
FEI Numbers
13
Registration Numbers
13
Same Product Code
27
Applicant Total
4
Review Days
296

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Basic Information

Device Name
CTS-3060 AUTOMATED SEMEN ANALYZER
K Number
K881765
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.5220
Medical Specialty
Hematology
Decision
Substantially Equivalent
Applicant
Motion Analysis Corp.
Date Received
April 25, 1988
Decision Date
February 15, 1989
Product Code
POV
Advisory Committee
Hematology
Review Advisory Committee
HE
Third Party
N

Classifications

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

Product Code Device Name
POV Semen Analysis Device

Similar 510(k) Clearances

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

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Other Clearances by Motion Analysis Corp.

K Number Device Name
K890076 ORTHOTRAK
K890075 FOOTTRAK
K890074 SPINETRAK