Atlas FDA

AMES TDA TM PHENYTOIN TEST

FDA 510(k) clearance K801736 · decided 1980-08-20

Clearance details

K-number
K801736
Device name
AMES TDA TM PHENYTOIN TEST
Applicant
Miles Laboratories, Inc.
Decision
Substantially Equivalent
Date received
1980-07-25
Decision date
1980-08-20
Days to decision
26 days
Clearance type
Traditional
Product code
LES
Device class
2
Regulation number
862.3350
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
IMMPULSE COATED TUBE PHENYTOIN ASSAY REAGENTS (K865102)Sclavo, Inc.1987-01-13
SYVA ADVANCE EMIT PHENYTOIN ASSAY (K844990)Syva Co.1985-01-23
STRATUS PHENYTOIN FLUOROMETRIC ENZYME (K831154)American Dade1983-05-16
SYVA ADVANCE SYS. EMIT,(R)-AED(R) PHENY (K820187)Syva Co.1982-02-12
PHENYTOIN FLUORESCENT IMMUNOASSAY (K813538)American Diagnostic Corp.1981-12-31
AMES TDA TM PHENYTOIN TEST (K811025)Miles Laboratories, Inc.1981-04-29

Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
BIOSTATOR GLUCOSE CONTROLLER (P800032/S001)Miles Laboratories, Inc.1983-06-02
BIOSTATOR GLUCOSE CONTROLLER (P800032)Miles Laboratories, Inc.1981-05-28