FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

GEN-PROBE PAL LUMINOMETER

K Number: K903911 · Decision Oct 4, 1990
Classifications
1
FEI Numbers
85
Registration Numbers
85
Same Product Code
257
Applicant Total
62
Review Days
41

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Basic Information

Device Name
GEN-PROBE PAL LUMINOMETER
K Number
K903911
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.2300
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Gen-Probe, Inc.
Date Received
August 24, 1990
Decision Date
October 4, 1990
Product Code
JJQ
Advisory Committee
Clinical Chemistry
Review Advisory Committee
CH
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
JJQ Colorimeter, Photometer, Spectrophotometer For Clinical Use

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Other Clearances by Gen-Probe, Inc.

K Number Device Name
K122062 APTIMA TRICHOMONAS VAGINALIS ASSAY - PANTHER
K111409 APTIMA COMBO 2 ASSAY
K063664 GEN-PROBE APTIMA ASSAY FOR NEISSERIA GONORRHOEAE MODEL#1091
K063451 GEN-PROBE APTIMA ASSAY FOR CHLAMYDIA TRACHOMATIS, MODEL 1199
K062440 GEN-PROBE APTIMA ASSAY FOR NEISSERIA GONORRHOEAE, MODEL 1091
K061413 APTIMA CT ASSAY ON THE TIGRIS DTS SYSTEM
K061509 TIGRIS DTS GEN-PROBE APTIMA ASSAY FOR NEISSERIA GONORRHOEAE, MODEL 1196
K060652 TIGRIS DTS GEN-PROBE APTIMA COMBO 2 ASSAY
K053446 GEN-PROBE APTIMA ASSAY FOR CHLAMYDIA TRACHOMATIS, MODEL 1088
K043224 GEN-PROBE APTIMA COMBO 2 ASSAY
Search all 62 clearances from Gen-Probe, Inc. →