FDA.report

510(k) K904173

Device
INSULATED ELECTRODES AND LAPAROSCOPIC PROBICS
Applicant
Baxter Healthcare Corp
510(k) number
K904173
Product code
HET
Decision
Substantially Equivalent (SESE)
Decision date
1990-12-10
Date received
1990-09-11
Regulation
884.1720
Classification name
Laparoscope, Gynecologic (And Accessories)
Medical specialty
Obstetrics/Gynecology
Review panel
Obstetrics/Gynecology
Device class
2
Clearance type
Traditional
Third party reviewed
N
Source
FDA openFDA 510(k) dataset plus migrated FDA.report data

Related Records

Applicant Contact

Contact
LAJUAN MCGILL
Address
7280 N. Caldwell Niles IL US 60648 60648

FDA Registration Numbers

Source Documents

FDA 510(k) Premarket Notification Database · 510(k) summary PDF not indicated by FDA · openFDA JSON

Related GUDID Devices

Primary DIBrandCompanyPublished
10885403051982V. MuellerCAREFUSION 2200, INC2016-09-24

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