510(k) K895713

Device
3m Igg Fastlyme(tm) Test
Applicant
3M COMPANY
510(k) number
K895713
Product code
LSR
Decision
Substantially Equivalent (SESE)
Decision date
1990-12-14
Date received
1989-09-25
Regulation
866.3830
Classification name
Reagent, Borrelia Serological Reagent
Medical specialty
Microbiology
Review panel
Microbiology
Device class
2
Clearance type
Traditional
Third party reviewed
No

Applicant Contact#

Contact
SYLVIA ZORICH
Address
3380 Central Expy. Santa Clara CA US 95051 95051

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

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