510(k) K810832

Device
Forecaster
Applicant
FORECASTER CO.
510(k) number
K810832
Product code
LHD
Decision
Substantially Equivalent (SESE)
Decision date
1981-06-24
Date received
1981-03-25
Classification name
Device, Fertility Diagnostic, Proceptive
Medical specialty
Unknown
Review panel
Unknown
Device class
U
Clearance type
Traditional
Third party reviewed
No

Applicant Contact#

Address
803 N. Front St. Suite 3 Mchenry IL US 60050 60050

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

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K952756MEDI-AID BASAL THERMOMETERPolymedica Industries, Inc.1995-09-25
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K880618FERTILITY FORECASTER COMPUTER PROGRAMFertile Time, Ltd.1988-06-24
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K870528OVU-TRAC OVULATION TIMING KITOb/Gyn Concepts, Ltd.1987-05-06
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