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510(k) K780237

Device
DISPOSABLE CONTROLLED DROP PASTEUR PIPET
Applicant
OWENS-ILLINOIS, INC.
510(k) number
K780237
Product code
GJG  
Decision
Substantially Equivalent (SESE)
Decision date
1978-03-09
Date received
1978-02-13
Regulation
864.6160
Classification name
Pipette, Quantitative, Hematology
Medical specialty
Hematology
Review panel
Hematology
Device class
1
Clearance type
Traditional
Third party reviewed
No

Applicant Contact#

Address
19 Leigh Fisher Blvd. El Paso TX US 79906 79906

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code GJG  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K831079LIQUIPETTEThe Kendall Company Div. of Tyco Healthcare Group1983-04-28
K781891PIPETTES, PLASTIC DISPOSABLEHillwood Corp.1978-11-15
K760719UNIFORM DROP SIZE PASTEUR TYPE PIPETSDade, Baxter Travenol Diagnostics, Inc.1976-10-29

Legacy Summary#

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FDA Review#

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