Atlas FDA

DIGOCTK 125

FDA 510(k) clearance K800773 · decided 1980-04-24

Clearance details

K-number
K800773
Device name
DIGOCTK 125
Applicant
Sorin Biomedica, Fiat, USA, Inc.
Decision
Substantially Equivalent
Date received
1980-04-07
Decision date
1980-04-24
Days to decision
17 days
Clearance type
Traditional
Product code
LCS
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
DIGOXIN COATED TUBE RIA (K922353)Monobind1992-08-24
QMS - DIGOXIN (K913562)Seradyn, Inc.1991-08-30
INNOFLUOR DIGOXIN REAGENT SET (K895828)Innotron of Oregon, Inc.1989-10-30
FIAGEN DIGOXIN TIME-RESOLVED FLUOROIMMUNOASSAY KIT (K884707)Cyberfluor, Inc.1989-01-17
IMMPULSE DIGOXIN ASSAY REAGENTS (K874748)Sclavo, Inc.1988-02-19
DART DIGOXIN ASSAY (K864802)Coulter Electronics, Inc.1987-02-12
TDX DIGOXIN (K820154)Abbott Laboratories1982-02-05
ULTRA-DIG (K812749)Antibodies, Inc.1981-10-19
I-125 LABELED DIGOXIN (K803047)Pcl-Ria, Inc.1980-12-22
DIGOXIN EIA KIT (K801490)M.A. Bioproducts1980-07-14
AMERLEX DIGOXIN RIA KIT (K801413)Amersham Corp.1980-07-08
DIGOXIN RADIOIMMUNOASSAY KIT (K801202)Technia Diagnostics , Ltd.1980-06-20

Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
AB-CORE K HEPATITIS B CORE ANTIGEN 125I (P850044/S003)Sorin Biomedica, Fiat, USA, Inc.1987-02-17
AB-CORE K HEPATITIS B CORE ANTIGEN 125I (P850044/S002)Sorin Biomedica, Fiat, USA, Inc.1986-10-31
AB-CORE K HEPATITIS B CORE ANTIGEN 125I (P850044/S001)Sorin Biomedica, Fiat, USA, Inc.1986-08-26