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510(k) K760750

Device
STERILE TUBULAR UNBLEACHED STOCKINETTE
Applicant
DENNISON MANUFACTURING CO.
510(k) number
K760750
Product code
JLG  
Decision
Substantially Equivalent (SESE)
Decision date
1976-10-08
Date received
1976-10-01
Regulation
862.1290
Classification name
Conversion To Ferric Hydroxymates (colorimetric), Fatty Acids
Medical specialty
Clinical Chemistry
Review panel
Clinical Chemistry
Device class
1
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

Other 510(k) Records For Product Code JLG  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K812081WAKO NEFA C TESTWako Chemicals USA, Inc.1981-08-12

Legacy Summary#

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FDA Review#

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