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510(k) K884974

Device
ACCESSORY TO EYEDROP GUIDE
Applicant
SUREDROP, INC.
510(k) number
K884974
Product code
JYJ  
Decision
Substantially Equivalent (SESE)
Decision date
1989-03-24
Date received
1988-11-30
Regulation
874.4420
Classification name
Gauge, Measuring
Medical specialty
Ear Nose & Throat
Review panel
Ear Nose & Throat
Device class
1
Clearance type
Traditional
Third party reviewed
No

Applicant Contact#

Contact
WILLIAM SMITH
Address
P.O. Box 123 Tiger GA US 30576 30576

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code JYJ  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K904469EYEOPENERKc Medical Industries1991-06-28
K874569SUREDROP EYEDROP GUIDESuredrop, Inc.1988-05-03
K833606IMPLANT MEASURING GAUGEMicrotek Medical, Inc.1984-01-03
K801938RHINOMETERAztec Medical Products, Inc.1980-09-09

Legacy Summary#

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FDA Review#

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