Atlas FDA

OPTIMATE DIGOXIN TEST

FDA 510(k) clearance K853021 · decided 1985-08-07

Clearance details

K-number
K853021
Device name
OPTIMATE DIGOXIN TEST
Applicant
Miles Laboratories, Inc.
Decision
Substantially Equivalent
Date received
1985-07-18
Decision date
1985-08-07
Days to decision
20 days
Clearance type
Traditional
Product code
DPB
Device class
2
Regulation number
862.3320
Medical specialty
Clinical Toxicology
Advisory committee
Clinical Toxicology
Location
Elkhart, IN, 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
DIGOXIN KIT (K823014)Pcl-Ria, Inc.1982-11-01
125I DIGOXIN RADIOIMMUNOASSAY KIT (K821811)Cambridge Medical Technology1982-07-02
DIGOXIN RADIOIMMUNOASSAY (K820274)American Diagnostic Corp.1982-02-23
DIGOXIN RADIOIMMUNOASSAY SYSTEM (K792153)Radioimmunoassay, Inc.1979-11-13
RIA, DIGNXIN-125-I (K790602)Endocrine-Metabolic Center1979-07-30
RIA TEST KIT, CENTRIA DIGOXIN (K790540)Ventrex Laboratories, Inc.1979-04-23
125I DIGOXIN TEST SET (K772306)Wien Laboratories, Inc.1977-12-22
125 I DIGOXIN RIA KIT (K771525)Diagnostic Products Corp.1977-10-14
DIGI-TAB-RIA DIGOXIN RADIOMMUNOASSAY (K760883)Nuclear Medical Laboratories, Inc.1976-11-19

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