Atlas FDA

RIA PHASE DIGOXIN

FDA 510(k) clearance K800205 · decided 1980-03-19

Clearance details

K-number
K800205
Device name
RIA PHASE DIGOXIN
Applicant
Boehringer Mannheim Corp.
Decision
Substantially Equivalent
Date received
1980-01-30
Decision date
1980-03-19
Days to decision
49 days
Clearance type
Traditional
Product code
DPO
Device class
2
Regulation number
862.3320
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
IMMULITE DIGOXIN (K914833)Cirrus Diagnostics, Inc.1991-11-22
ECLIPSE ICA DIGOXIN (K905719)Biotope, Inc.1991-01-17
DIGOXIN/RIA KIT COATED TUBE RADIOIMMUNOASSAY KIT (K864449)Canadian Bioclinical, Ltd.1987-02-02
RIA COAT DIGOXIN (K833842)Immuno Assay Corp.1984-01-17
SOPHEIA DIGOXIN EIA KIT (K832163)Diagnostic Products Corp.1983-08-12
IMMUCHEM COVALENT-COAT RIA KIT (K830962)Immuchem Corp.1983-05-04
COAT-A-COUNT DIGOXIN RIA (K811932)Diagnostic Products Corp.1981-07-23
KALLESTAD QUANTICOAT 125 DIGOXIN (K811776)Kallestad Laboratories, Inc.1981-07-10
AUTOPAK 12 DIGOXIN TEST DELIVERY SYSTEM (K791325)Micromedic Systems1979-08-16
VENTRE/SEP DIGOXIN RADIOIMMUNOASSAY KIT (K791355)Ventrex Laboratories, Inc.1979-08-10
IGOXIN SOLID PHASE RIA (K771638)Bd Becton Dickinson Vacutainer Systems Preanalytic1977-10-07
RADIOIMMUNOASSAY DIGOXIN TEST, IN VITRO (K770365)Travenol Laboratories, S.A.1977-02-24

Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
ENZYMUN TEST{R} CEA (P860058/S001)Boehringer Mannheim Corp.1993-07-29
ENZYMUN-TEST{R} AFP (P860044/S003)Boehringer Mannheim Corp.1991-09-03
ENZYMUN-TEST{R} AFP (P860044/S002)Boehringer Mannheim Corp.1991-07-19
ENZYMUN-TEST{R} AFP (P860044/S001)Boehringer Mannheim Corp.1990-08-03
MICUR-MIC SYSTEMS (P820073)Boehringer Mannheim Corp.1983-06-29