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

PHOTON IMMUNOASSAY ANALYZER

K Number: K832364 · Decision Aug 26, 1983
Classifications
1
FEI Numbers
85
Registration Numbers
85
Same Product Code
257
Applicant Total
63
Review Days
39

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
PHOTON IMMUNOASSAY ANALYZER
K Number
K832364
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.2300
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Hybritech, Inc.
Date Received
July 18, 1983
Decision Date
August 26, 1983
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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (JJQ), ordered by most recent decision date.

View all

Other Clearances by Hybritech, Inc.

K Number Device Name
K972666 TANDEM-MP OSTASE IMMUNOENZYMETRIC ASSAY
K961573 TANDEM-R OSTASE IMMUNORADIOMETRIC ASSAY
K930810 TANDEM-R OSTASE IMMUNORADIOMETRIC ASSAY
K922754 TANDEM-E IGE II CALIBRATION VERIFICATION SET
K921745 HYBRITECH STRATUS PAP FLUOROMETRIC ENZYME IMMUNO
K921252 TANDEM-E FERRITIN CALIBRATION VERIFICATION CONROL
K920556 TANDEM-E HCG CALIBRATION VERIFICATION CONTROL SET
K921763 TANDEM ICON QSR CKMB IMMUNOENZYMETRIC ASSAY
K912439 TANDEM-E TSH CALIBRATION VERIFICATION CONTROL SET
K911417 ICON STREP B IMMUNOENZYMETRIC ASSAY
Search all 63 clearances from Hybritech, Inc. →