510(k) K860350

Device
SERUM CHOLINESTERASE REAGENT SET
Applicant
STERLING DIAGNOSTICS, INC.
510(k) number
K860350
Product code
DLI  
Decision
Substantially Equivalent (SESE)
Decision date
1986-04-24
Date received
1986-01-30
Regulation
862.3240
Classification name
Acetylcholine Chloride, Specific Reagent For Pseudo Cholinesterase
Medical specialty
Toxicology
Review panel
Clinical Chemistry
Device class
1
Clearance type
Traditional
Third party reviewed
No

Applicant Contact#

Contact
DAVID L CALLENDER
Address
34210 Dequindre Rd. Sterling Heights MI US 48077 48077

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code DLI  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K950180DUPONT DIMENSION(R) PSEUDOCHOLINESTERASE METHODE.I. Dupont DE Nemours & Co., Inc.1995-03-15
K930208CHOLINESTERASE METHOD FOR TECHNICON CHEM1/TECHNICOHeraeus Kulzer, Inc.1993-04-20
K860641EASY-TEST (CHE) REAGENT, ITEM NO. 67522/93Em Diagnostic Systems, Inc.1986-04-03
K833062SERUM CHOLINESTERASE REAGENT SETSterling Biochemical, Inc.1983-11-25
K771024CHOLINESTERASE REAGENT SYSTEMAmerican Monitor Corp.1977-07-15

Legacy Summary#

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FDA Review#

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