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510(k) K831105

Device
Cordia Pap
Applicant
CORDIS CORP.
510(k) number
K831105
Product code
JFH
Decision
Substantially Equivalent (SESE)
Decision date
1983-05-16
Date received
1983-04-05
Regulation
862.1020
Classification name
Acid Phosphatase (Prostatic), Tartrate Inhibited
Medical specialty
Clinical Chemistry
Review panel
Clinical Chemistry
Device class
2
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 JFH#

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K000257IMMULITE 2000 PAP, MODELS L2KPA2, L2KPA6Diagnostic Products Corp.2000-02-23
K981573UBI MAGIWEL PAP (PROSTATIC ACID PHOSPHATASE) EIA QUANTITATVEUnited Biotech, Inc.1998-09-15
K964756PROSTATIC ACID PHOSPHATASE REAGENT TEST/PROSTATIC ACID PHOSPHATASE REAGENT KITWano-Tech Corp.1997-04-23
K931701IMMULITE PAPDiagnostic Products Corp.1994-01-27
K925377IMX PAPAbbott Laboratories1993-01-13
K921745HYBRITECH STRATUS PAP FLUOROMETRIC ENZYME IMMUNOHybritech, Inc.1992-07-30
K902937MILENIA PAP IRMA CATALOG #: MKPA1, XDiagnostic Products Corp.1990-09-21
K901933COAT-A-COUNT PAP IRMA, CATLOG# 1KPA1, 1KPA2Diagnostic Products Corp.1990-06-28
K895723IRMA-COUNT(TM) PAP, (RKPA1, RKPA2)Diagnostic Products Corp.1989-10-31
K893508PROSTATE SPECIFIC ANTIGEN IMMUNOHISTOCHEMICAL ANTIBaxter Healthcare Corp1989-08-04
K884748TECHNICON CHEM 1 SYSTEM ACID PHOS (PROSTATIC)Technicon Instruments Corp.1989-01-30
K873903ABBOTT PAP-EIAAbbott Laboratories1987-12-01
K864945TANDEM(R) M-PAK(TM) PAP IMMUNOENZYMETRIC ASSAYHybritech, Inc.1987-01-05
K863832NAPHTHYL PHOSPHATE, ACID PHOSPHATASEPointe Scientific, Inc.,1986-12-16
K852845PROSTATIC ACID PHOSPHATASE RADIOIMMUNOASSAYDiagnostic Products Corp.1985-09-04