Atlas FDA

THEOPHYLLINE KIT FLUORESCENCE POLARIZA-

FDA 510(k) clearance K842585 · decided 1984-09-26

Clearance details

K-number
K842585
Device name
THEOPHYLLINE KIT FLUORESCENCE POLARIZA-
Applicant
Windsor Laboratories, Inc.
Decision
Substantially Equivalent
Date received
1984-07-03
Decision date
1984-09-26
Days to decision
85 days
Clearance type
Traditional
Product code
LER
Device class
2
Regulation number
862.3880
Medical specialty
Clinical Toxicology
Advisory committee
Clinical Toxicology
Location
Mchenry, IL, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
THEOPHYLLINE FPIA REAGENT SET AND CALIBRATORS (K942192)Sigma Diagnostics, Inc.1994-07-13
CEDIA(R) THEOPHYLLINE ASSAY/MODIFICATION (K905521)Microgenics Corp.1990-12-26
TURBOX THEOPHYLLINE ASSAY (K882570)Unipath , Ltd.1988-11-10
IMMPULSE COATED TUBE THEOPHYLLINE ASSAY REAGENTS (K864409)Sclavo, Inc.1986-12-22
THEOFAST(TM) TEST PACKAGE (K863475)3M Company1986-11-05
IMMPULSE THEOPHYLLINE ASSAY REAGENTS (K840758)Paragon Diagnostics, Inc.1984-04-04
TDX THEOPHYLLINE (K833070)Abbott Laboratories1983-11-14
AMWA TDA THEOPHYLLINE TEST (K831514)Miles Laboratories, Inc.1983-06-30
COBAS STANDARD FOR TOTAL PROTEIN (K823576)Hoffmann-La Roche, Inc.1983-01-07
AMERIFLUOR THEOPHYLLINE FLUORESCENT IMM (K820397)American Diagnostic Corp.1982-03-02
EMIT-AAD THEOPHYLLINE ASSAY (K813240)Syva Co.1981-12-03
AMES TDA THEOPHYLLINE TEST (K812518)Miles Laboratories, Inc.1981-09-23

Recalls involving this device

No recalls on record reference this clearance.